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Article

Genomic Structure, Protein Character, Phylogenic Implication, and Embryonic Expression Pattern of a Zebrafish New Member of Zinc Finger BED-Type Gene Family

by
Chih-Wei Zeng
1,†,
Jin-Chuan Sheu
1 and
Huai-Jen Tsai
2,3,*
1
Liver Disease Prevention and Treatment Research Foundation, Taipei 100008, Taiwan
2
School of Medicine, Fu Jen Catholic University, New Taipei City 242062, Taiwan
3
Department of Life Science, Fu Jen Catholic University, New Taipei City 242062, Taiwan
*
Author to whom correspondence should be addressed.
†
Current address: Department of Molecular Biology, UT Southwestern Medical Center, 6000 Harry Hines Blvd, Dallas, TX 75390, USA.
Genes 2023, 14(1), 179; https://doi.org/10.3390/genes14010179
Submission received: 7 November 2022 / Revised: 22 December 2022 / Accepted: 4 January 2023 / Published: 9 January 2023
(This article belongs to the Section Animal Genetics and Genomics)
Browse Figures
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Abstract

:
We reported a new member of the C2H2-zinc-finger BED-type (ZBED) protein family found in zebrafish (Danio rerio). It was previously assigned as an uncharacterized protein LOC569044 encoded by the Zgc:161969 gene, the transcripts of which were highly expressed in the CNS after the spinal cord injury of zebrafish. As such, this novel gene deserves a more detailed investigation. The 2.79-kb Zgc:161969 gene contains one intron located on Chromosome 6 at 16,468,776–16,475,879 in the zebrafish genome encoding a 630-aa protein LOC569044. This protein is composed of a DNA-binding BED domain, which is highly conserved among the ZBED protein family, and a catalytic domain consisting of an α-helix structure and an hAT dimerization region. Phylogenetic analysis revealed the LOC569044 protein to be clustered into the monophyletic clade of the ZBED protein family of golden fish. Specifically, the LOC569044 protein was classified as closely related to the monophyletic clades of zebrafish ZBED4-like isoforms and ZBED isoform 2. Furthermore, Zgc:161969 transcripts represented maternal inheritance, expressed in the brain and eyes at early developmental stages and in the telencephalon ventricular zone at late developmental stages. After characterizing the LOC569044 protein encoded by the Zgc:161969 gene, it was identified as a new member of the zebrafish ZBED protein family, named the ZBEDX protein.

1. Introduction

A zinc finger is a small structural motif with one or more coordinated zinc ions (Zn2+). The zinc finger protein consists of several structural families based on their different three-dimensional structures, among which the C2H2-type zinc finger motif is the most common structure among the classic C2H2-type zinc finger proteins. Some C2H2-type zinc finger proteins were reported to play an important role in zebrafish development. For example, the C2H2-type zinc finger protein 16-like protein regulates oligodendrocyte specification, migration, and myelination during zebrafish embryo development [1]. The C2H2-type zinc finger protein insulinoma-associated 1 promotes zebrafish CaP motor neuron development through Olig2 and Nkx6.1 [2], and the C2H2-type zinc finger transcription factor (sp7) promotes skeletogenesis [3].
The C2H2-zinc-finger BED-type (ZBED) gene represents another zinc finger protein family type. The ZBED protein family is widely expressed in vertebrate tissues, consisting of numerous genes and sharing a unique and conserved BED domain that binds to the DNA element. This domain was discovered from two chromatin-boundary-element-binding proteins, Drosophila BEAF and DREF, using bioinformatics analysis [4]. The BED domain comprises 50–60 amino acid residues with two highly conserved aromatic positions, sharing cysteines and histidine to form a zinc finger. Except for the conserved BED domain, each ZBED gene has its own unique domain. Therefore, each member within the ZBED protein family may play its own distinct biological function, e.g., the ZBED2 protein is acquired during pancreatic ductal adenocarcinoma (PDA) progression to suppress the IFN pathway, resulting in the promotion of PDA tumor proliferation [5]. The ZBED3 protein is involved in carcinogenesis and embryogenesis owing to its interaction with Axin, which is vital for Wnt/β–catenin signal modulation in mammals [6]. The ZBED4 mRNA is exclusively expressed in glial Müller cells and human retina cone photoreceptors [7]. The ZBED6 protein also binds to the target insulin-like growth factor-2 (IGF2) motif and inhibits IGF2 expression, resulting in the promotion of cell proliferation, growth, and development [8]. Therefore, searching for more novel member(s) within the ZBED protein family will allow us to comprehensively understand the family’s characteristics.
In particular, we took advantage of the zebrafish (Danio rerio) model to search for a novel member of the ZBED family that controls neurogenesis during the embryonic stage. After analyzing gene information generated from spinal cord-injured zebrafish embryos by RNA-Seq Transcriptome analysis [9], we found a transcript from an unknown zebrafish gene assigned as the Zgc:161969 gene that was highly expressed in the CNS. Based on amino acid sequence and evolutionary tree analyses, we identified that the uncharacterized LOC569044 protein encoded by the Zgc:161969 gene was a zebrafish ZBED protein, which turned out to be a new member of the zinc finger BED-type protein family, named zebrafish ZBEDX. Taking this a step further, we clearly defined the ZBEDX gene and its encoded ZBEDX protein in terms of genomic and protein information, phylogenetic implication, and embryonic expression patterns. Interestingly, we revealed that ZBEDX mRNA is maternally inherited and expressed at high levels during neuronal development at an early embryonic stage.

2. Materials and Methods

2.1. Ethics Statement

The animal protocol, which was strictly followed in this study, was reviewed and approved by the Institutional Animal Care and Use Committee (IACUC) of the Fu Jen Catholic University with ethics approval number A11064.

2.2. Zebrafish Husbandry and Microscopy

The zebrafish AB strain was cultured as previously described [10]. The embryos were grown at 28.5 °C in embryo media (EM), staged, and fixed as described by Westerfield (2000) [10]. Pigmentation in the embryos was inhibited by supplementing EM with 0.003% 1-phenyl 2-thiourea (PTU) (MiliporeSigma, Darmstadt, Germany) at 24 h post-fertilization (hpf) [11]. The embryos were observed under a light stereomicroscope (MZ FLIII, Leica, Bensheim, Germany).

2.3. Sequence Alignments

All published sequences from different species were obtained from GenBank (https://www.ncbi.nlm.nih.gov/genbank/, accessed on 1 March 2021). The deduced amino acid sequences of the ZBED domain of zebrafish Zgc:161969 (uncharacterized protein LOC569044; NP_001077318.1), ZBED1-like (XP_021327416.1), ZBED4 (XP_002666517.2), ZBED4-like (XP_001340716.5), ZBED4-like isoform 1 (XP_005165631.1), ZBED4-like isoform 2 (XP_005165631.1), ZBED isoform 1 (NP_001373713.1) and ZBED isoform 2 (NP_001373714.1) were obtained from the National Center for Biotechnology Information (NCBI) nucleotide and protein database. First, the sequences in the FASTA mode were mapped in a motif search in GenomeNet (https://www.genome.jp, accessed on 1 March 2021) to identify the protein domains and key residues using the Pfam software 35.0 [12] and InterPro database (https://www.ebi.ac.uk/interpro/, accessed on 1 March 2021). Next, we blasted the BED domain in NCBI and identified an uncharacterized protein (LOC569044; GenBank accession number: NM_001083849.1).

2.4. Phylogenetic Tree and Homology Analyses

A phylogenetic tree was constructed using the Phylogeny.fr (www.phylogeny.fr, accessed on 1 March 2021) platform based on information about the zebrafish ZBED family from Ensembl (www.ensembl.org, accessed on 1 March 2021) and ZFIN (www.zfin.org, accessed on 1 March 2021). MUSCLE v5, DNA Data Bank of Japan (DDBJ), and ClustalW/X (the version is 2.1) were utilized for multiple alignments: PhyML for tree building and TreeDyn for tree drawing [13,14]. The amino acid sequence encoded by Zgc:161969 (NP_001077318.1) was deduced, and its phylogenetic tree was determined in two ways, as follows:
(1)
Based on the full-length amino acid sequence: the alignment between LOC569044 and other members in the ZBED family of known species, including Homo sapiens ZBED4 (AAI67155.1), E3 SUMO-protein ligase ZBED1 (NP_001164606.1) and ZBED1 (AAH15030.1); Rattus norvegicus ZBED4 (XP_032775174.1); Mus musculus ZBED4 (NP_852077.1); Xenopus tropicalis ZBED1 (XP_004911791.1), and ZBED1 isoform X1 (XP_012813067.2); Carassius auratus ZBED1-like (XP_026072939.1), ZBED1-like isoform X1 (XP_026117831.1), ZBED1-like isoform X2 (XP_026117841.1), ZBED4-like (XP_026116228.1), ZBED4-like isoform X1 (XP_026069790.1), ZBED4-like isoform X2 (XP_026069791.1), ZBED4-like isoform X3 (XP_026117848.1), and Triplophysa tibetana ZBED4 (KAA0713175.1).
(2)
Based on the BED domain: the alignment between LOC569044 and other known species, including H. sapiens ZBED5 (NP_001137139.1), Transposase-like protein (AAF18454.1), Transcription factor IIIA (NP_002088.2), DNA/RNA-binding protein (AAA75623.1), and Xenopus transcription factor IIIA homologue (BAA06988.1); M. musculus Transcription factor IIIA isoform CRA a (EDL05819.1) and Transcription factor IIIA isoform CRA b (EDL05820.1); X. tropicalis PR domain zinc finger protein 15 isoform X1 (XP_012813515.1); C. auratus ZBED1-like (XP_026072939.1), ZBED4-like isoform X1 (XP_026117831.1), Trichohyalin-like (XP_026072553.1), ZBED1-like isoform X1 (XP_026117831.1), Zinc finger protein 319-like isoform X1 (XP_026084591.1) and Putative transposase (AFC96943.1); T. tibetana ZBED4 (KAA0712498.1), and Zinc finger protein 1 (KAA0710290.1).

2.5. Protein Structure Prediction

The topological elements of secondary and tertiary structures of ZBED proteins were predicted with Robetta (http://robetta.bakerlab.org/, provided by the Baker lab, HHMI’s Janelia Research Campus, accessed on 1 August 2021) [15] using default parameters.

2.6. RNA Extraction, cDNA Synthesis, Polymerase Chain Reaction (PCR), and Antisense mRNA Probe Synthesis

The tissues were homogenized, frozen in TRIzol reagent (15596026, Invitrogen), and stored at −80 °C. The total RNA extraction was performed according to Zeng et al. (2022) [16,17]. In summary, 2 μg of RNA were reverse transcribed into cDNA using the Transcriptor First Strand cDNA Synthesis Kit (Roche Molecular Systems, Pleasanton, CA, USA). The synthesized cDNA was stored at −20 °C. All PCR amplifications were carried out in 50-μL reactions using specific primers. We generated the RNA probe by reverse transcribing the DNA fragments already cloned into a pCS2 vector. For ZBEDX, 1800 base pairs were amplified by PCR using the forward primer (5′-TATATCTAGAGGATCCATGGAGAGATCTCGTACAGC-3′) and reverse primer (5′-TATACTCGAGTTATTCCAAAGTGGAGATGATTTTGC-3′). The gene encoding this protein was subsequently cloned.

2.7. Whole-Mount In Situ Hybridization (WISH)

WISH was performed as described by Zeng et al. (2016) [18] and Lee et al. (2017) [19] with some modifications. Digoxigenin (DIG)-labeled RNA antisense probe was synthesized from linearized plasmid using the DIG RNA Labeling Kit (SP6/T7) (Roche). After permeabilization, zebrafish embryos at the stages of 1-cell, 2-cell, 24-, 48-, 72-, and 96-hpf were hybridized with the probe overnight and incubated with an anti-DIG antibody (Roche; 1:8000 times dilution). Positive signals were observed under a light stereomicroscope (MZ FLIII, Leica, Bensheim, Germany).

3. Results and Discussion

3.1. A New Member of the ZBED Protein Family Encoded by Zebrafish Zgc:161969

Gene Zgc:161969 was screened from the RNA-seq transcriptomic source generated by the spinal cord injury of zebrafish. Since it showed a highly increased expression during spinal cord injury, it was determined to be involved in neuronal regeneration [9] for this study. However, neither the Zgc:161969 gene nor its encoded protein LOC569044 has been completely characterized: a task we performed in this work.
The 2.79-kb Zgc:161969 gene consists of one intron located on chromosome 6 at 16,468,776–16,475,879 in the zebrafish genome (Ensembl number ENSDARG00000041359.7). The full-length cDNA of Zgc:161969 contains 1890 nucleotide base pairs (bp) encoding 633 amino acid residues [National Center for Biotechnology Information (NCBI) GenBank accession number: NM_001083849.1; Figure 1A]. Using Pfam software and the InterPro database to predict putative major domains, we found that the LOC569044 protein encoded by Zgc:161969 contained a ZBED domain located at amino acid residues from 17 to 59 (Figure 1A).
Upon checking both potential transcripts from NCBI, the result showed that both transcripts XM_005168715 and NM_0010838491 are predicted from D. rerio zgc:161969 (zgc:161969), transcript variant X1, mRNA (717 amino acids), D. rerio zgc:161969 (zgc:161969), and mRNA (630 amino acids), respectively. After using the standard protein BLAST of both proteins predicted from the NCBI database, we found that the percentage of the full-length NM_0010838491 protein alignment with XM_005168715 was a 93% identity. The alignment result showed that the different region between them was only a few amino acids located at the N-terminal site (Supplementary Figure S1; green color). Since both potential transcripts contain an essential ZBED domain (Supplementary Figure S1; yellow color), we suggested that both potential transcripts belonged to the ZBED protein family. However, those different parts of sequences are still undefined, which might provide us with an interesting topic for future study. In this study, we used XM_005168715 and NP_001077318.1 as reference sequences from NCBI.
To future investigate whether the Zgc:161969 gene is synteny in conservation across bony fishes or to other vertebrates, we performed the genomic alignments of 65 bony fishes. The results revealed a very low degree of synteny between the zebrafish LOC569044 protein and that of the other bony fish we compared. However, a little similar alignment sequence located at chromosome 6 was found in three species of bony fish, which included Sinocyclocheilus grahami, Astyanax mexicanus, and Ictalurus punctatus (Supplementary Figure S2). Additionally, we could not find any syntenic conservation in humans. Based on these results, we suggested that (1) the Zgc:161969 has a very low degree of synteny conservation across bony fishes and other vertebrates, and (2) the Zgc:161969 has its own unique amino acid sequence.
Since the LOC569044 protein encoded by Zgc:161969 in zebrafish possesses a BED domain which is an essential and evolutionarily conserved DNA-binding domain in the ZBED protein family, we further characterized the biological property of this protein using a comparative protein approach. We first examined whether the LOC569044 protein encoded by the Zgc:161969 gene co-evolved with other proteins in the zebrafish ZBED protein family. After the NCBI Standard protein BLAST of more than 20 zebrafish ZBED proteins predicted from the NCBI database, we did not align any known ZBED proteins that shared a highly similar protein sequence, suggesting that the LOC569044 protein encoded by Zgc:161969 has its own unique amino acid sequence, except for containing a BED domain which is a highly conserved domain within the zebrafish ZBED protein family (Figure 1B). When the deduced amino acid sequence of LOC569044 was compared with that of all known zebrafish ZBED proteins, we found that it shared 37, 67, 58, 50, 50, 52, and 54% identity with zebrafish ZBED1-like, ZBED4, ZBED4-like, ZBED4-like isoform 1, ZBED4-like isoform 2, ZBED isoform 1, and ZBED isoform 2, respectively (Table 1). Specifically, the protein sequence of LOC569044 was relatively similar to that of ZBED4 and ZBED4-like isoforms. On the other hand, when the phylogenetic analysis was performed, we found that two major monophyletic clades were categorized within the ZBED protein family of the zebrafish and that the LOC569044 protein was classified as related to the monophyletic clades of ZBED4-like isoforms and ZBED isoform 2 (Figure 1A).
Except for the typical BED domain, we went further to analyze another conserved domain, the hAT dimerization region, of the LOC569044 protein and compared it with that of zebrafish ZBED proteins. It has been reported that ZBED proteins may have been domesticated from transposases in one or two independent regions [4]. DNA transposon in the hAT superfamily is widespread in animals, including several active and well-studied elements, such as the Ac transposon of Zea mays, the hobo transposon of Drosophila melanogaster, the Hermes transposon of the housefly Musca domestica, and the Tol2 transposon of the Japanese medaka fish (Oryzias latipes) [20,21]. When we compared the LOC569044 protein with other ZBED proteins in zebrafish using Pfam software 35.0, we found that the LOC569044 protein contained a hAT dimerization domain located at amino acid residues from 423 to 512 (Figure 1B). The hAT transposons and related domesticated sequences constitute a large superfamily that was recently characterized [22]. Similar to many members of the zebrafish ZBED family proteins, the LOC569044 protein was found to belong to the hAT transposon superfamily.
Based on protein sequence identity, conserved BED and hAT dimerization domains, and phylogenetic analysis, we concluded that the LOC569044 protein encoded by Zgc:161969 is a new member of the ZBED protein family in zebrafish, designated as the ZBEDX protein.

3.2. Prediction of ZBEDX Protein Structure

ZBED proteins have recently been characterized by signature Cx2CxnHx3−5[H/C] (xn is a variable spacer). The amino acid sequence of the BED domain of the ZBED protein was compared with that of seven ZBED proteins in zebrafish, such as ZBED isoform 1_I (first ZBED domain), ZBED isoform 1_II (second ZBED domain), ZBED isoform 2, ZBED 4, and ZBED4-like isoform 1_I (Figure 2A). Based on the amino acid sequence alignment of the zinc-finger regions of these seven ZBED proteins in zebrafish, the conserved region Cx2CxnTxnHx4Lx2KH was found to be shared (Figure 2A, red star and yellow). We noticed that the zinc-finger region of this novel ZBEDX protein also contained the conserved C2C19T5HL2KH region.
We also employed WebLogos (version 2.8.2, https://weblogo.berkeley.edu/, accessed on 1 August 2021) to compare the consensus amino acid residue of the ZBEDX protein and seven other known ZBED proteins in zebrafish. The results demonstrated that similar to the seven ZBED proteins in zebrafish, ZBEDX contains a conserved zinc-finger BED domain-containing seven consensus amino acid residues CCTHLTH (Figure 2(Bi)). Additionally, when we compared the nucleic acid sequence of the hAT dimerization region of the ZBEDX protein with those of seven ZBED proteins in zebrafish, four consensus nucleic acids TTAA (TA-rich) were found (Figure 2(Bii)). A TA-rich sequence is required for the integration of each transposon. Thus, a greater number of TA-rich consensus sequences should enhance the chance that transposon could have in finding a site to integrate [23]. The recent characterization of ZBED proteins shows the presence of two highly conserved aromatic amino acids: tryptophan and phenylalanine [24]. However, ZBEDX contains 5% phenylalanine and 1% tryptophan, suggesting that the ZBEDX protein contains one zinc-finger region of the BED domain, a TA-rich hAT dimerization region, and a highly conserved aromatic amino acid, phenylalanine.
In general, the main function of the zinc-finger region of the BED domain is to bind DNA elements. However, its other functions include the binding of RNA, proteins, and small molecules [25]. In fact, structural changes in the BED domain might alter the binding specificity of a particular protein [26]. Therefore, the secondary structure of the ZBED protein might help us understand how ZBED interacts with DNA, RNA, or proteins. We investigated protein structure prediction using Robetta (see Materials and Methods), and the ZBEDX protein-predicted model was found to be a helix-rich representative structural model separated into two major regions (Figure 2C). One was an N-terminal BED domain consisting of a helix–turn–helix motif near the N-terminus formed by amino acid residues from 1 to 168 and a zinc-finger region. The zinc-finger region could be further classified into several structural families, and each one has a unique three-dimensional architecture [27]. Therefore, we speculated that the helix–turn–helix motif of ZBEDX may be a binding region for DNA, RNA, or proteins. Another region was the catalytic domain consisting of several helix–turn–helix motifs containing β-sandwich structures near the C-terminus formed by amino acid residues from 169 to 633. This domain included over ten helix–turn–helix motifs and was composed of α-helical domains and a hAT dimerization region which may require the activation, repression, or epigenetic control of DNA [22]. This line of evidence indicated that the ZBEDX protein contained a BED domain at the N-terminal domain, as well as α-helical domains and a hAT dimerization region at the catalytic domain, suggesting that the predicted secondary structure of ZBEDX was consistent with the secondary structures of other proteins within the ZBED family.

3.3. Phylogenetic Analysis of Zebrafish ZBEDX Protein

To examine the evolutionary relationship between teleost and other species of the ZBED family, we constructed a phylogenetic tree based on the full-length deduced entire amino acid sequence of the zebrafish ZBEDX protein. The results demonstrated that the zebrafish ZBEDX found in this study were clustered into the Osteichthyes (bony fish) monophyletic group (Figure 3). When the deduced amino acid sequence of zebrafish ZBEDX was compared with sequences of other species in the ZBED family, we found that the zebrafish ZBEDX shared (1) 22, 75, 75, 20, 75, 82, and 81% identity with bony fish C. auratus ZBED1-like, ZBED1-like isoform X1, ZBED1-like isoform X2, ZBED4-like, ZBED4-like isoform X1, ZBED4-like isoform X2, and ZBED4-like isoform X3, respectively. In addition, it shared (2) 21 and 20% identity with amphibian X. tropicalis ZBED1, and ZBED1 isoform X1, respectively; (3) 20, 24, and 21% identity with human Homo sapiens ZBED4, E3 SUMO-protein ligase ZBED1 and ZBED1, respectively; and (4) 21% identity with M. musculus and Rattus rattus (Table 2). Based on these results, we concluded that zebrafish ZBEDX is evolutionarily close to the ZBED family of bony fish.
Next, we used phylogenetic analysis to compare the ZBEDX and ZBED proteins found in multiple bony fishes. The result showed the ZBEDX clustered into ZBED4 monophyletic group (Figure 4). However, ZBEDX was a more distantly related group of organisms (outgroup), without any ZBED protein in the same clade, suggesting that zebrafish ZBEDX has its own unique amino acid sequence not only presented in zebrafish per se but also presented in other bony fish (Figure 4). After the Standard protein BLAST of ZBED proteins of multiple bony fishes predicted from the NCBI database, we found that the percentage of the full-length ZBEDX protein alignment with multiple bony fishes were 84, 83, and 83% identity with the Ctenopharyngodon idella ZBED4 isoform X2, Cyprinus carpio ZBED4-like isoform X2, and ZBED4-like isoform X3, respectively (Table 3). Taken together, we conclude that zebrafish ZBEDX is (1) evolutionarily close to the ZBED family of bony fishes and (2) clustered into the monophyletic clade and outgroup of the ZBED protein family of multiple bony fishes.
The number of BED domains varies among ZBED family proteins in zebrafish. For example, ZBED isoform 2, ZBED4, and ZBED4-like isoform 2 contain a single BED domain, while ZBED isoform 1 and ZBED4-like isoform 1 contain two BED domains (Figure 1A). The new member ZBEDX protein discovered in this study contains a single BED domain similar to that of ZBED isoform 2, ZBED4, and ZBED4-like isoform 2. However, the number of BED domains among ZBED family proteins in humans is relatively wide-ranging. For example, human ZBED1 contains a single BED domain, ZBED6 has two BED domains, and ZBED4 contains four BED domains, while the human ZBED6 C-terminal-like protein (C7ORF29) is completely absent of BED domain, possibly from the loss of its original BED domain or the failure to insert ancestrally active transposons during evolution [28]. Thus, investigating the evolutionary mechanisms leading to the occurrence of variable numbers of BED domains among the ZBED family proteins would be an interesting question for further study.
Regarding the context of the BED domain, we employed phylogenetic trees to analyze the amino acid sequences of the BED domain of mammals, amphibians, and bony fish. The results demonstrated that the BED domain of ZBEDX was categorized into a specific monophyletic clade in which the transcription factor IIIA family of mammals, such as the M. musculus Transcription factor IIIA (TFIIIA) isoform CRA and H. sapiens TFIIIA, was included (Figure 5). The human TFIIIA is a single protein that contains zinc and possesses a repetitive C2H2 zinc finger domain to regulate the transcription of the 5S ribosomal RNA gene [29]. On the other hand, we noticed that the BED domain of zebrafish ZBEDX shared the same monophyletic clade with that of zebrafish ZBED4-like isoforms and ZBED isoform 2 (Figure 1). However, the BED domains of ZBED4-like isoforms and ZBED isoform 2 were also grouped into the same monophyletic clade as that of the human Transposase-like protein (Figure 5). Although the teleost and other vertebrates contain a conserved BED domain among ZBED proteins categorized into the same monophyletic clade, the above results suggest that the total amino acid sequence of the BED domain is not necessarily identical or even similar, resulting in different biological functions.

3.4. Temporospatial Expression of ZBEDX mRNA in Zebrafish Embryos

To examine the temporospatial expression of zebrafish ZBEDX transcripts, WISH was performed on zebrafish embryos collected from 24, 48, 72, and 96 hpf. The data demonstrated that zebrafish ZBEDX transcripts were detectable as early as the one- and two-cell stages (Figure 6A–D), suggesting that ZBEDX mRNAs were transmitted into oocytes through maternal inheritance. Later on, from 24 to 72 hpf, ZBEDX transcripts were specifically distributed in the forebrain, midbrain, hindbrain, retinae, and branchial arches (Figure 6E–M). Since ZBEDX transcripts were detected in the central nervous system and eyes during embryonic development, it is highly likely that the ZBEDX protein might be involved in developing these tissues during embryogenesis in zebrafish. Moreover, ZBEDX transcripts were detected explicitly in the ventricular zone (VZ) of the brain at 48 hpf (Figure 6N–P). At 72 hpf, ZBEDX transcripts were mainly displayed in the telencephalon VZ, where cells proliferated actively before eventually migrating to the mantle zone [30]. Some embryonic neuronal stem/progenitor cells (NSPCs) in VZ may also possess similar proliferation.

4. Conclusions

This study is the first report to define a previously uncharacterized LOC569044 protein encoded by the uncharacterized zebrafish gene Zge:161969. Based on the deduced amino acid sequence alignment, protein structure, and phylogenetic analyses, we confirmed that the LOC569044 protein is (1) composed of a DNA-binding BED domain and a catalytic domain; (2) clustered into the monophyletic clade of the ZBED protein family of fish; and (3) classified as closely related to the monophyletic clades of zebrafish ZBED4-like isoforms and ZBED isoform 2. This line of evidence suggests that the zebrafish LOC569044 protein encoded by the Zge:161969 gene is a new member of the zebrafish zinc finger BED-type protein family, designated as the zebrafish ZBEDX protein. Meanwhile, we also studied the expression patterns of ZBEDX transcripts in the zebrafish embryos at various developmental stages and found that they are mainly distributed in the brain, spinal cord, and eyes. Specifically, ZBEDX transcripts are maternally inherited.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/genes14010179/s1, Figure S1. The deduced amino acid sequences of two potential transcripts and one uncharacterized protein LOC569044; Figure S2. Comparison of the gene maps encoding zebrafish LOC569044 protein and those of multiple bony fishes.

Author Contributions

C.-W.Z. and H.-J.T. designed, carried out experiments, and co-wrote the paper. C.-W.Z. prepared all materials and performed bioinformatic analysis in this study. J.-C.S. and H.-J.T. conceived and designed the research and data interpretation, helped edit the manuscript, and served as PIs to apply for funding. All authors have read and agreed to the published version of the manuscript.

Funding

This work was partially supported by the Ministry of Science and Technology, Taiwan, ROC, under grant no. 110-2313-B-030-002, and partially supported by the Liver Disease Prevention and Treatment Research Foundation, Taipei, Taiwan.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the IACUC, Mackay Medical College, Taiwan, with approval number MMC-A1070011 (27 March 2019).

Informed Consent Statement

Not applicable.

Data Availability Statement

The data supporting the findings of this study are available from the corresponding authors upon request.

Acknowledgments

We are very grateful for the support of Spencer Lee and Hsiao-Ching Nien of the Liver Disease Prevention and Treatment Research Foundation, Taipei, Taiwan.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. The essential domains of the ZBED protein family in zebrafish and their phylogenetic tree. (A) Different domains were labeled by various colors as indicated. Arabic numbers represent the position of amino acid residues located at each domain, while Roman numerals presented in circles indicate the number of zinc finger BED domains existing in ZBED proteins. (B) Phylogenetic tree for ZBED proteins in zebrafish (transcript ID in Table 1). Three monophyletic clades indicated by different colors are categorized. The uncharacterized LOC569044 protein encoded by the Zgc:161969 gene is marked by a black box.
Figure 1. The essential domains of the ZBED protein family in zebrafish and their phylogenetic tree. (A) Different domains were labeled by various colors as indicated. Arabic numbers represent the position of amino acid residues located at each domain, while Roman numerals presented in circles indicate the number of zinc finger BED domains existing in ZBED proteins. (B) Phylogenetic tree for ZBED proteins in zebrafish (transcript ID in Table 1). Three monophyletic clades indicated by different colors are categorized. The uncharacterized LOC569044 protein encoded by the Zgc:161969 gene is marked by a black box.
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Figure 2. Comparison of the amino acid sequences of ZBED domain between LOC569044 protein and other zebrafish ZBED proteins. (A) The alignment of amino acids of BED domains among zebrafish ZBED proteins. The DNA-binding BED domain was characterized by the signature Cx2CxnHx3-5H (xn indicates a variable spacer; yellow color). Blue color indicates that at least one amino acid residue among zebrafish ZBED proteins was identical to that of LOC569044 protein, while the red color indicates amino acid residue in all zebrafish ZBED proteins entirely identical to that of the LOC569044 protein. *: indicates that the amino acid residue is identical among all species examined. (B) Using the WebLogos (version 2.8.2) to analyze the consensus residues of amino acid and nucleic acid of conserved zinc finger BED domain (i) and hAT dimerization region (ii), respectively. The larger size of alphabetic letters represent a higher degree of consensus. (C) A predicted protein structure of LOC569044 protein. Four views of the predicated protein structures were demonstrated by a 180-degree rotation. Positions of N- and C-termini are labeled. Positions of the three domains are labeled by red boxes, and a hAT dimerization region is labeled by pink box.
Figure 2. Comparison of the amino acid sequences of ZBED domain between LOC569044 protein and other zebrafish ZBED proteins. (A) The alignment of amino acids of BED domains among zebrafish ZBED proteins. The DNA-binding BED domain was characterized by the signature Cx2CxnHx3-5H (xn indicates a variable spacer; yellow color). Blue color indicates that at least one amino acid residue among zebrafish ZBED proteins was identical to that of LOC569044 protein, while the red color indicates amino acid residue in all zebrafish ZBED proteins entirely identical to that of the LOC569044 protein. *: indicates that the amino acid residue is identical among all species examined. (B) Using the WebLogos (version 2.8.2) to analyze the consensus residues of amino acid and nucleic acid of conserved zinc finger BED domain (i) and hAT dimerization region (ii), respectively. The larger size of alphabetic letters represent a higher degree of consensus. (C) A predicted protein structure of LOC569044 protein. Four views of the predicated protein structures were demonstrated by a 180-degree rotation. Positions of N- and C-termini are labeled. Positions of the three domains are labeled by red boxes, and a hAT dimerization region is labeled by pink box.
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Figure 3. Phylogenetic analysis of the LOC569044 protein and the ZBED proteins found in mammals, amphibians, and bony fish. The full amino acid sequences of ZBED proteins from the known species are human (H. sapiens), mouse (M. musculus), zebrafish (D. rerio), frog (X. tropicalis), goldfish (C. auratus), and stone loach (T. tibetana), which were used to characterize the LOC569044 protein. ZBED proteins from known species were categorized into three main monophyletic clades labeled in different colors (transcript ID in Table 2). The LOC569044 protein marked by a black box was categorized in the same monophyletic group, along with the ZBED of bony fish (in green). The scale bar represents the number of substitutions per site. The blue and red colors indicate the same monophyletic group in the mammals and amphibians in, respectively.
Figure 3. Phylogenetic analysis of the LOC569044 protein and the ZBED proteins found in mammals, amphibians, and bony fish. The full amino acid sequences of ZBED proteins from the known species are human (H. sapiens), mouse (M. musculus), zebrafish (D. rerio), frog (X. tropicalis), goldfish (C. auratus), and stone loach (T. tibetana), which were used to characterize the LOC569044 protein. ZBED proteins from known species were categorized into three main monophyletic clades labeled in different colors (transcript ID in Table 2). The LOC569044 protein marked by a black box was categorized in the same monophyletic group, along with the ZBED of bony fish (in green). The scale bar represents the number of substitutions per site. The blue and red colors indicate the same monophyletic group in the mammals and amphibians in, respectively.
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Figure 4. Phylogenetic analysis of the LOC569044 protein and ZBED protein found in multiple bony fishes. The full-length amino acid sequences of ZBED proteins from different species of bony fishes, such as C. clupeaformis, T. tibetana, M. asiaticus, X. texanus, C. carpio, C. idella, and M. amblycephala used to characterize the LOC569044 protein. The LOC569044 protein is marked by a rectangular box. The scale bar represents the number of substitutions per site.
Figure 4. Phylogenetic analysis of the LOC569044 protein and ZBED protein found in multiple bony fishes. The full-length amino acid sequences of ZBED proteins from different species of bony fishes, such as C. clupeaformis, T. tibetana, M. asiaticus, X. texanus, C. carpio, C. idella, and M. amblycephala used to characterize the LOC569044 protein. The LOC569044 protein is marked by a rectangular box. The scale bar represents the number of substitutions per site.
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Figure 5. Phylogenetic analysis of the LOC569044 protein and the ZBED domains found in mammals, amphibians, and bony fish. The full amino acid sequences of ZBED domains in ZBED proteins from the known species are human (H. sapiens), mouse (M. musculus), zebrafish (D. rerio), frog (X. tropicalis), goldfish (C. auratus), and stone loach (T. tibetana), which were used to characterize the LOC569044 protein. The LOC569044 protein is marked by a black box. The proteins labeled in the same color are recognized as a group of proteins that are close in evolution and function of BED domains. Scale bar represents the number of substitutions per site.
Figure 5. Phylogenetic analysis of the LOC569044 protein and the ZBED domains found in mammals, amphibians, and bony fish. The full amino acid sequences of ZBED domains in ZBED proteins from the known species are human (H. sapiens), mouse (M. musculus), zebrafish (D. rerio), frog (X. tropicalis), goldfish (C. auratus), and stone loach (T. tibetana), which were used to characterize the LOC569044 protein. The LOC569044 protein is marked by a black box. The proteins labeled in the same color are recognized as a group of proteins that are close in evolution and function of BED domains. Scale bar represents the number of substitutions per site.
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Figure 6. Expression pattern of ZBEDX transcripts during the early developmental stages of zebrafish embryos. Embryos at different stages, as indicated, were collected and hybridized with antisense probe against ZBEDX mRNA using whole-mount in situ hybridization. Panels (A,C,E,H,K,N) are lateral views, while panels (B,D,F,I,J,L,M,O,P) are dorsal views. Panels (E,H,K,N) are lateral views, and the anterior of embryos was placed at the left, while panels (G,J,M,P) are dorsal views, and the anterior of embryos is on the top. At 12 hpf, ZBEDX transcripts were expressed in whole embryo. ZBEDX transcripts were initially apparent at the 1- (A,B) and 2-cell (C,D) stages. At 24–72 hpf, ZBEDX transcripts were expressed in forebrain (f), midbrain (m), hindbrain (h), retina (r), spinal cord (sc), and branchial arches (ba) (E–M). At 96-hpf, ZBEDX transcripts were expressed in midbrain (m) and hindbrain (h) (N–P).
Figure 6. Expression pattern of ZBEDX transcripts during the early developmental stages of zebrafish embryos. Embryos at different stages, as indicated, were collected and hybridized with antisense probe against ZBEDX mRNA using whole-mount in situ hybridization. Panels (A,C,E,H,K,N) are lateral views, while panels (B,D,F,I,J,L,M,O,P) are dorsal views. Panels (E,H,K,N) are lateral views, and the anterior of embryos was placed at the left, while panels (G,J,M,P) are dorsal views, and the anterior of embryos is on the top. At 12 hpf, ZBEDX transcripts were expressed in whole embryo. ZBEDX transcripts were initially apparent at the 1- (A,B) and 2-cell (C,D) stages. At 24–72 hpf, ZBEDX transcripts were expressed in forebrain (f), midbrain (m), hindbrain (h), retina (r), spinal cord (sc), and branchial arches (ba) (E–M). At 96-hpf, ZBEDX transcripts were expressed in midbrain (m) and hindbrain (h) (N–P).
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Table
Table 1. The identity (in percentage) of deduced amino acid residues of novel LOC569044 protein compared with those of seven known ZBED proteins found in zebrafish.
Table 1. The identity (in percentage) of deduced amino acid residues of novel LOC569044 protein compared with those of seven known ZBED proteins found in zebrafish.
SpeciesNameTranscript IDLength (aa)Total Identity
(%) a		BED Domain Identity (%) b
D. rerioLOC569044 (Zgc:161969 gene)BC134839.1630100100
ZBED1-likeXP_021327416.16611937
ZBED4XP_002666517.26362567
ZBED4-likeXP_001340716.56502058
ZBED4-like isoform 1XP_005165631.19762650
ZBED4-like isoform 2XP_005165631.18872650
ZBED isoform 1NP_001373713.14013452
ZBED isoform 2NP_001373714.12632654
Note: a The query cover described how many (in %) amino acid (aa) residues in the full-length of novel LOC569044 protein are identical with those of the known zinc finger BED domain-containing protein members in zebrafish; b The identity (in %) of aa residues contained in the BED domain among zebrafish ZBED proteins.
Table
Table 2. The identity (in percentage) of deduced amino acid residues of the ZBEDX protein compared with those of known ZBED proteins found in higher vertebrates.
Table 2. The identity (in percentage) of deduced amino acid residues of the ZBEDX protein compared with those of known ZBED proteins found in higher vertebrates.
SpeciesNameTranscript IDLength (aa)Identity (%) a
D. rerioZBEDX (Zgc:161969 gene)NP_001077318.1630100
C. auratusZBED1-likeXP_026072939.162822
ZBED1-like isoform X1XP_026117831.172975
ZBED1-like isoform X2XP_026117841.166775
ZBED4-likeXP_026116228.163120
ZBED4-like isoform X1XP_026069790.172275
ZBED4-like isoform X2XP_026069791.163582
ZBED4-like isoform X3XP_026117848.164281
H. sapiensZBED4AAI67155.1117120
E3 SUMO-protein ligase ZBED1NP_001164606.169424
ZBED1AAH15030.169421
M. musculusZBED4NP_852077.1116821
R. rattusZBED4XP_032775174.1117021
X. tropicalisZBED1XP_004911791.163921
ZBED1 isoform X1XP_012813067.269320
Note: a The query cover describes how many (in %) amino acid (aa) residues in the full-length of novel ZBEDX protein are identical with those of known BED domain-containing ZBED proteins found in higher vertebrates.
Table
Table 3. The identity (in percentage) of deduced amino acid residues of the ZBEDX protein compared with those of known ZBED proteins found in bony fishes.
Table 3. The identity (in percentage) of deduced amino acid residues of the ZBEDX protein compared with those of known ZBED proteins found in bony fishes.
SpeciesNameTranscript IDLength (aa)Identity (%) a
D. rerioZBEDX
(Zgc:161969 gene)		NP_001077318.1630100
Coregonus clupeaformisZBED4-likeXP_041752989.262351
T. tibetanaZBED4KAA0713175.162268
Myxocyprinus asiaticusZBED 4-like isoform X1XP_051540434.163769
ZBED 4-like isoform X2XP_051540435.163669
uncharacterized protein LOC127415457XP_051510176.162767
Xyrauchen texanusZBED 4-likeXP_051973224.163669
ZBED4-like isoform X1XP_051950732.162767
C. idellaZBED4 isoform X1XP_051752038.174978
ZBED4 isoform X2XP_051752039.166284
ZBED4 isoform X3XP_051752040.165478
Megalobrama amblycephalaZBED4 isoform X1XP_048056422.173078
ZBED4 isoform X3XP_048056424.172478
ZBED4 isoform X4XP_048056425.171678
C. carpioZBED4-like isoform X1XP_042613966.172277
ZBED4-like isoform X2XP_018955884.163583
ZBED4-like isoform X3XP_018927958.263783
Note: a The query cover describes how many (in %) amino acid (aa) residues in the full-length of novel ZBEDX protein were identical with those of known BED domain-containing ZBED proteins found in higher vertebrates. The gray column shows the top three high identity percentages of aa residues in the full-length novel ZBEDX protein compared to multiple bony fishes.
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Zeng, C.-W.; Sheu, J.-C.; Tsai, H.-J. Genomic Structure, Protein Character, Phylogenic Implication, and Embryonic Expression Pattern of a Zebrafish New Member of Zinc Finger BED-Type Gene Family. Genes 2023, 14, 179. https://doi.org/10.3390/genes14010179

AMA Style

Zeng C-W, Sheu J-C, Tsai H-J. Genomic Structure, Protein Character, Phylogenic Implication, and Embryonic Expression Pattern of a Zebrafish New Member of Zinc Finger BED-Type Gene Family. Genes. 2023; 14(1):179. https://doi.org/10.3390/genes14010179

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Zeng, Chih-Wei, Jin-Chuan Sheu, and Huai-Jen Tsai. 2023. "Genomic Structure, Protein Character, Phylogenic Implication, and Embryonic Expression Pattern of a Zebrafish New Member of Zinc Finger BED-Type Gene Family" Genes 14, no. 1: 179. https://doi.org/10.3390/genes14010179

APA Style

Zeng, C. -W., Sheu, J. -C., & Tsai, H. -J. (2023). Genomic Structure, Protein Character, Phylogenic Implication, and Embryonic Expression Pattern of a Zebrafish New Member of Zinc Finger BED-Type Gene Family. Genes, 14(1), 179. https://doi.org/10.3390/genes14010179

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