Detection of Polymorphisms in the MTNR1A Gene and Their Association with Reproductive Performance in Awassi Ewes
by
, , ,
Giovanni Cosso
1
,
Michella Nehme
2,
Sebastiano Luridiana
1,
Luisa Pulinas
1,
Giulio Curone
3
,
Chadi Hosri
4,
Vincenzo Carcangiu
1 and
Maria Consuelo Mura
1,*
1
Department of Veterinary Medicine of Sassari, University of Sassari, Via Vienna 2, 07100 Sassari, Italy
2
Department of Agriculture and Food Engineering, Faculty of Engineering, Holy Spirit University of Kaslik, Kaslik, Jounieh 446, Lebanon
3
Department of Veterinary Medicine of Milan, University of Milan, Via dell’Università 6, 26900 Lodi, Italy
4
Department of Veterinary Sciences, Faculty of Agriculture, Lebanese University, Dekwaneh, Beirut 14/6573, Lebanon
*
Author to whom correspondence should be addressed.
Animals 2021, 11(2), 583; https://doi.org/10.3390/ani11020583
Submission received: 19 January 2021
/
Revised: 9 February 2021
/
Accepted: 18 February 2021
/
Published: 23 February 2021
(This article belongs to the Section Animal Reproduction)
Abstract
:Simple Summary
The purpose of the study was to explore the influence of MTNR1A gene polymorphisms on the reproductive performance in Awassi sheep, which is an important and widespread breed in developing Mediterranean countries. A total of 31 SNPs was detected, 5 of which caused amino acid changes. Two of the found SNPs were found to be totally linked and associated with an advanced reproductive recovery in ewes carrying the C allele. The obtained results could be useful for improving reproductive management in developing Mediterranean areas.
Abstract
The economy in Mediterranean areas is tightly linked to the evolution of the sheep-farming system; therefore, improvement in ewe’s reproductive performance is essential in the developing countries of this area. MTNR1A is the gene coding for Melatonin receptor 1 (MT1), and it is considered to be involved in the reproductive activity in sheep. The aims of this study were: (1) identifying the polymorphisms from the entire MTNR1A coding region and promoter in Lebanese Awassi sheep flocks, and (2) investigating the association between the found polymorphisms and the reproductive performance, assessed as lambing rate, litter size, and days to lambing (DTL). The study was conducted in two districts of Lebanon, where 165 lactating ewes, aged 5.2 ± 1.5 years, with body condition score (BCS) 3.3 ± 0.4, were chosen and exposed to adult and fertile rams. From 150 to 220 days after ram introduction, lambing dates and litter sizes were registered. This study provided the entire coding region of the MTNR1A receptor gene in the Awassi sheep breed. Thirty-one single nucleotide polymorphisms (SNPs) were detected, five of which were missense mutations. The H2, H3, and H4 haplotypes were associated with lower DTL (p < 0.05), as well as the SNPs rs430181568 and rs40738822721, named from now on SNP20 and SNP21, respectively. These SNPs were totally linked and can be considered as a single marker. The ewes carrying the C allele at both these polymorphic sites advanced their reproductive recovery (p < 0.05). These results are essential for improving reproductive management and obtaining advanced lambing in Awassi ewes.
1. Introduction
Small ruminants residing in temperate latitudes rely upon the photoperiod as a time signal to synchronize their reproductive activity with the external environment [1]. Changes in day length are perceived by the retina and translated into a chemical signal by the pineal gland through nocturnal secretion of melatonin [2]. Therefore, secretion and blood concentrations of melatonin are low during daylight hours and high at night-time; this is an organic medium that informs ruminants of photoperiods [3,4]. In mammalian reproduction, melatonin determines its effect at different levels of the hypothalamic, pituitary, and gonadal axis via specific receptors [5,6].
There are three melatonin receptor subtypes, which belong to the superfamily of G protein-coupled receptors [7]; these receptor subtypes are melatonin receptor 1A (MT1), melatonin receptor 1B (MT2), and melatonin receptor 1C (MT3). These subtypes’ coding genes have been cloned [8] and mapped in several animal species [9]. The melatonin receptor 1A (MTNR1A) gene is located on Chromosome 26 in sheep. It extends from the 17,354,820 to 17,377,973 position of the Oar_rambouillet_v1.0 genome assembly and consists of two exons, separated by an intron nearly 22 kilo-bases (kb) in length. The exons I and II of the MTNR1A gene are approximately 260 and 970 baise-pair (bp) in length, respectively. The MTNR1A locus exhibits several polymorphic sites, which are associated with seasonal reproductive activity in ewes [10,11], goats [12,13], buffalos [14], and wild animals [15]. Whilst the effects of the MTNR1A gene on reproductive seasonality studied so far are related to three specific mutations found in the exon II, at positions 606, 612, and 706 [16,17], the other parts of this gene have only been investigated in Sarda and Aragonese sheep [18]. These studies on the entire MTNR1A gene in these two breeds have provided confirmation of the influence of this gene in the control of reproductive seasonality and new knowledge useful for improving the reproductive management of sheep farms. Considering that the economy of many Mediterranean areas is greatly linked to the evolution of the sheep-farming system, it would be beneficial to characterize the MTNR1A gene sequence in the Awassi sheep, which is a very widespread breed in the Mediterranean area [19,20]. The opportunity to control and manage reproductive seasonality is a strong tool for economic growth in developing countries. Therefore, the first aim of this study was to identify the polymorphisms from the entire MTNR1A coding region and promoter in Lebanese Awassi sheep flocks. The second aim of this study was to investigate the association between the found polymorphisms and the reproductive performance of the sheep flocks.
2. Materials and Methods
2.1. Ethical Approval
Animals used in this research were managed and treated by the farm’s veterinary service in accordance with the European Commission’s recommendations. An explicit ethical agreement was not necessary as blood samples were taken by the National Health Veterinary Service during routine flock health control procedures. Sheep were included in this trial with the farmers’ permission.
2.2. Animals and Management
The study was conducted in two districts of Lebanon—Bekaa and Jezzine—located in the northeast and south of Lebanon respectively. In each district, a sheep farm was selected, each raising approximately 200 Awassi ewes that had been exposed to natural photoperiods since birth.
The Bekaa Plain stretches from Mount Lebanon to Anti-Lebanon, the altitude of which ranges from 600 to 1100 m. The plain is divided into two climatic regions: (1) the north with a sub-desert climate where the average annual temperature is 17 °C, with low rainfall ranging from 200 to 400 mm and (2) the south where the average annual temperature is 15 °C, with higher rainfall ranging from 900 to 1000 mm. Alternatively, in the Jezzine Coastal Plain the average annual temperature is 19 °C and the rainfall ranges from 700 to 1000 mm per year. The rainfall in Lebanon is notably high during the winter, and concentrated from November to February. In contrast, the summer is very dry, particularly in the north of the Bekaa. In both districts, the farming was of the semi-extensive type. Animals usually remain in and around the farm with low use of rangelands. Pastures are usually located near to the farm, and the flocks have short daily movement that allows them to return each evening to their farm. They depend on crop residue plots when available. In order to compensate for low forage quality and/or availability, and the negative effects induced by climatic conditions (summer drought from June to October and winter cold from December to January), ewes were provided with a daily cereal-based supplement. The most common food supplement for flocks in these farms included barley, yellow corn, and wheat, which were fed either whole or cracked.
On 20 June 2017, 165 lactating ewes (89 in Bekaa district and 76 in Jezzine) aged 3–8 years (5.2 ± 1.5 years), with body condition score (BCS) 2.5–4.0 (3.3 ± 0.4), were chosen. Their BCS on a 1 to 5 scale [21] were assessed on June 10.
2.3. Reproductive Data Collection
From 1 July 2017 to 30 August 2017, the 89 ewes in Bekaa and the 76 ewes in Jezzine districts were, respectively, exposed to five and four adult rams. The health of the rams was confirmed by a veterinarian, and they were proven to be fertile as they had produced offspring in previous breeding seasons. The timing of the exposure ensured that lambing occurred between late November and the end of January. From 150 to 220 days after ram introduction, lambing dates and litter size were registered. From the recorded data, lambing rate (number of lambed ewes per ewe exposed to the ram), litter size (number of new-born lambs per lambed ewes), and days to lambing (DTL, i.e., number of days between the joining of rams until the subsequent lambing) were calculated.
2.4. Genotyping
From the jugular vein of each ewe, 10 mL of blood was collected using sterile vacuum tubes (BD Vacutainer System, Belliver Industrial Estate, Plymouth, UK) with ethylenediamine tetraacetic acid (EDTA) as an anticoagulant.
DNA extraction protocols and all the used primers for the amplifications of the promoter genomic region, exon I, exon II, and partial 3′ UTR were those reported by Luridiana et al. [22]. The polymerase chain reaction (PCR) and the electrophoresis conditions were performed following Luridiana et al. [22]. All PCR products were sequenced in forward and reverse direction by a commercial service (BioFab Research, Roma, Italy). Information about primers used for fragment amplification and PCR conditions are available in supplementary files Tables S1 and S2.
The found sequences were subjected to Nucleotide Blast (www.ncbi.nlm.nih.gov/blast/, accessed on 19 January 2021) for the alignment with the latest sheep genome assembly (Oar_rambouillet_v1.0—GenBank assembly accession number: GCF_002742125.1).
Bioedit Sequence Alignment Editor software (http://www.mbio.ncsu.edu/BioEdit/BioEdit.html, 19 January 2021) was used to align nucleotides.
2.5. Statistical Analysis
Allele frequency was obtained by direct counting of the found genotypes. The chi-squared test was used to determine the Hardy–Weinberg equilibrium of the variations (Genepop 4.2). R statistical software (Version 4.0.0) [23] was used to analyze the associations between each genotype (three levels), and reproductive traits—namely, the lambing rate, litter size, and DTL. Haplotype association studies, by Rpackage Haplo.stats [24] were used to evaluate the reproductive performances in each of the identified haplotypes. The same linear model was used for genotypes and haplotypes:
where Yjklm is the trait measured for each animal, µ is the overall mean, Gj is the fixed effect of the genotype (j = 3 levels, the 2 homozygotes and the heterozygote) or haplotype (j = 5 levels, H1 to H5), Ak is the age of each animal (k = 6 levels, 3–8), Dl is the random effect of the farming district (l = 2 levels, Bekaa and Jezzine), GjAk is the interaction between genotype or haplotype and age, and ejkl is the random residual effect of each observation. To compare number of ewes lambed each 10 days, we used a χ2 test. Statistical significance was set at p < 0.05 using the Bonferroni method at α = 0.05.
Yjklm = µ + Gj + Ak + Dl + GjAk + ejklm
3. Results
The obtained amplified and sequenced fragments corresponded to the exons I and II coding regions, to the promoter, to part of intron I, and the 3′ UTR region. From the sequence analysis, 31 single nucleotide polymorphisms (SNPs) were detected, and accordingly named SNP1–SNP31 (Table 1). The allele and genotype frequency, SNP identification code (ID), and p-values of the Hardy–Weinberg equilibrium are shown in Table 1. All genotype positions were inserted according to the last sheep genome assembly version (Oar_Rambouillet_v1.0, with accession RefSeq GCF_002742125.1). The identified SNPs were as follows: 15 in the promoter region; 1 in the intron I; 1 in the exon I; 10 in the exon II; and 4 in the 3′ UTR. Genotype distributions in SNP9 and SNP14 (promoter), in intron I, in exon I and II, and in 3′ UTR were in Hardy–Weinberg (HW) equilibrium. The other SNPs within the promoter region were not in equilibrium due to their high heterozygosity. On the other hand, SNP12 and SNP15 were in HW disequilibrium due to the low heterozygosity. Among all the SNPs, five were missense, which were within the exon II.
All of the SNPs causing an amino acid change were predicted as tolerated by variant effect predictor (VEP); their sorting intolerant from tolerant (SIFT) scores (to predict the effect of an amino acid substitution on protein function) were as follows: SNP17 = 0.27; SNP21 = 0.37; SNP22 = 0.22; SNP24 = 0.12; and SNP25 = 1. The SNP20 (rs430181568) and SNP21 (rs407388227) were totally linked (D’ = 1 and r2 = 1), so that they can be considered as a single marker.
All the SNPs were analyzed to evaluate their relationship with lambing rate, litter size, and DTL. The overall mean and the standard deviation (SD) for DTL and litter size in the enrolled ewes were 168.6 ± 19.4 and 1.1 ± 0.15, respectively; the lambing rate of the studied population was 0.87. A graphical representation about the distribution of each phenotypic trait based on age of enrolled ewes is shown in the Supplementary files (Figures S1–S3).
Statistical analysis showed that the C/C and T/C genotypes in SNP20 (rs430181568) and SNP21 (rs407388227) were associated with a shorter DTL, whilst litter size and lambing rate were not associated with the genotypes (Table 2). None of the other SNPs exhibited association with the analyzed reproductive traits. All the haplotypes with a frequency higher than 0.05 were considered in the haplotype association study for a total of five haplotypes, identified with the numerical code H1–H5, as shown in Table 3. The haplocodes H2, H3, and H4 were associated with lower DTL (p < 0.05) (Table 4). Litter size and lambing rate did not show statistical significance in the five haplotypes.
4. Discussion
The Awassi sheep is the most widespread, medium-sized breed of the Middle East, raised for milk and meat production. Its importance derives mainly from the easy adaptation to the hard environmental conditions; they endure well in the high temperatures, dietary fluctuation, and parasites infestation. Under extensive conditions, the mating period occurs in early summer and first lambing after 20 months of age. The ewes enrolled in this study were 3 to 8 years old, so that they were at least at their second lambing.
The genetic variability emerging from the MTNR1A gene sequences in the Awassi ewes is near to that found in the Sarda breed, however, there are some differences from the Raza Aragonesa breed [18,22]. Thirty one SNPs were identified in this study, compared to the 29 SNPs identified in the Sarda breed thus far, and the differences were observed at exon II and the promoter level. The five polymorphic sites causing amino acid changes among Awassi ewes were the same as those reported among the Sarda breed [22]. Alternatively, Calvo et al. [18] detected 12 additional SNPs causing amino acid changes within the exon II among the Raza Aragonesa breed. The analysis of the Awassi exon II sequence showed that the SNP20 (old 612/MnlI; rs430181568) was always associated with the SNP21 (rs407388227), which was coherent with that found in other European breeds [17,25]. This suggests that one or both SNPs may be involved in the regulation of reproductive seasonality [26]. The SNP21 (rs407388227) was found to cause an amino acid change (Val > Ile) in position 220 of the protein chain (GenBank access number AAB17721.1). This change is in the fifth transmembrane domain (TM5), which is a crucial site for the MT1a receptor functionality [27]. Missense mutations within this domain lead to important changes in signal transmission [28,29]. Furthermore, significant differences in cAMP inhibition among sheep with Val220 and Ile220 were observed [16], thus suggesting a possible change in melatonin signal transmission in sheep carrying different alleles at SNP21 (rs407388227). These variations in the melatonin signal perception could lead to the phenotype differences in reproductive recovery observed in this study.
However, it should be considered that the sample size may have influenced the effect of SNPs on the analyzed phenotypic traits (DTL, litter size, and lambing rate). In particular, a larger sample size could evidence associations between other SNPs and the recorded reproductive traits, although in a previous study on another sheep breed using a higher number of ewes, no other associations were found [22]. Moreover, ewes carrying the T/T genotype at SNP20/SNP21 (rs430181568/rs407388227) delayed the onset of their reproductive activity compared to the C/C and C/T ewes. This delay led to the different DTL recorded in this study, suggesting that among the observed ewes, there were differences in sensitivity to photoperiod. Furthermore, the identification of melatonin receptors in granulosa and other ovary cells confirms that melatonin plays an important role in different ovarian functions [30]. In the preovulatory follicular fluid, the recorded melatonin concentrations were approximately threefold higher than in the bloodstream [31]. These melatonin levels are presumably blood-derived, although precursors and enzymes for the synthesis of melatonin are found also in the ovary, and therefore it cannot be excluded that this organ also cooperates in the production of indolamine [32,33]. Melatonin administration has been shown to significantly counteract the apoptosis of granulosa cells through its antioxidant activity [31,34]. Some of these effects of melatonin on the granulosa cells are carried out through the decrease in the expression of some pro-apoptosis genes, and with the increase in the expression of other anti-apoptosis genes [35]. Both MT1 and MT2 receptors have been detected in granulosa cells, suggesting that the above effects could be carried out through the binding of melatonin receptors [31]. Recent studies have shown that silencing of receptor MT1 increases follicular atresia by increasing the expression of the anti-apoptosis genes [36]. Furthermore, the same research reported that in granulosa cells the expression of the GPX4 and SOD1 genes was inhibited after the silencing of the MT1 receptor, thus indicating that this receptor mediates the positive effect of melatonin on the expression of antioxidant genes.
Progesterone is essential for a regular estrus cycle and for the maintenance of pregnancy after ovulation [37]. Furthermore, progesterone production is directly related to the size of the ovarian follicle, with the highest secretion of this hormone from the granulosa cells in the larger ovarian follicles [38]. Melatonin increases the diameter of the corpus luteum, therefore increasing plasma progesterone concentrations [39]. The presence of melatonin receptors in the ovarian follicle suggests that melatonin can exert a direct control on the ovary [7,40]. It has been reported that melatonin induces progesterone secretion in granulosa cells, which appears partly to be due to MTNR1A, as the silencing of this receptor significantly reduces progesterone production [36,41]. Therefore, the inhibitory effect of melatonin on apoptotic genes, and its stimulatory effect on antioxidant genes and progesterone production, carried out through the MT1 receptor, is able to influence reproductive activity in sheep. So, as the different polymorphisms in SNP20 (rs430181568) and SNP21 (rs407388227) can influence the melatonin signal transmission, as mentioned above, it follows that even at the ovarian level, this could change the reproductive response of ewes. The lower DTL shown by ewes carrying the C/C or C/T genotype at SNP21 could be carried out by melatonin through a potential antiapoptotic and antioxidant effect via the MT1 receptor. This effect could safeguard the follicle development, thus causing an advanced reproductive resumption. In contrast, the longer DTL recorded in T/T ewes might depend on a limited follicle development.
The data analysis additionally highlighted that the presence of at least one C allele was enough to determine a positive effect on reproductive recovery. These findings are coherent with previous research involving different breeds of sheep [42,43]. The haplotype analysis equally supports this finding, since H2, H3, and H4, which all exhibited the C allele at positions 20 and 21 (corresponding to SNP20-rs430181568 and SNP21-rs407388227, respectively), are associated with a shorter DTL.
The fertility rate was not affected by polymorphisms of the MTNR1A gene, although we expected at least SNP21 (rs407388227) would influence the fertility rate as registered in other breeds [17,26]. This fact leads to several considerations that could explain the lack of effect of this polymorphism on sheep fertility. The first consideration that must be made is that the effect of this polymorphism on reproductive activity is marginal in this breed of sheep. This fact agrees with what was reported by Hernandez et al. [44] in the Ile de France breed, where the SNP20 (rs430181568) (which is totally linked to the SNP21, rs407388227) did not influence the reproductive activity. These authors suggested that the influence of this polymorphism on the regulation of reproductive seasonality depends on the sheep breed and/or environmental conditions. Another hypothesis could be that in the present study the ram introduction in the flock occurred after the photoperiod inversion, so that the ewes could be in a shallower anestrous state and be more sensitive to the ram effect. Thus, in the present research, lambings began to occur around December 15 overall in the ewes carrying the C/C and C/T genotypes, indicating that these ewes were more ready to resume reproductive activity at the ram introduction. Over time, the effect of the photoperiod became stronger leading the T/T ewes to resume their reproductive activity. Therefore, at the end of the observations, all the genotypes showed the same fertility rate.
5. Conclusions
This study provided the entire coding region of the MTNR1A receptor gene in the Awassi sheep breed. Thirty-one polymorphic sites were identified, five of which caused amino acid changes. The genotype and haplotype analysis highlighted that the presence of only one C allele in SNP20 (rs430181568) and SNP21 (rs407388227) is enough to advance reproductive recovery in this breed of sheep. Moreover, the above SNPs were totally linked and might be considered as markers for practical application in the selection of this trait. These results are therefore a valuable tool for improving reproductive management and obtaining advanced lambing in Awassi ewes. In order to better understand the effect of melatonin on the ovary, it would be useful to investigate whether the ewes carrying at least one C allele at SNP20 (rs430181568) and SNP 21 (rs407388227) show changes in the expression of genes promoting follicular development and the antioxidant effect at the ovarian level.
Supplementary Materials
The following are available online at https://www.mdpi.com/2076-2615/11/2/583/s1, Figure S1. The mean and the standard deviation of DTL divided by age, in the studied Lebanese Awassi population (n = 165), Figure S2. The mean and the standard deviation of litter size divided by age, in the studied Lebanese Awassi population (n = 165), Figure S3. Fertility rate (%) divided by age, in the studied Lebanese Awassi population (n = 165); Table S1. MTNR1A gene amplified regions and used primers, Table S2: PCR conditions for MTNR1A studied regions.
Author Contributions
All authors have made substantial contributions to all of the following: the conception and design of the study, acquisition of data, analysis and interpretation of data, and drafting the article and revising it critically for important intellectual content. All the authors approved the final version to be submitted. All authors have read and agreed to the published version of the manuscript.
Funding
This research was supported by grants from the RAS research project entitled RIPROGENOV and by University research fund 2019.
Institutional Review Board Statement
All the animals in this research had Lebanese Health Veterinary Service care in accordance with the Animal Welfare Act. Blood samples were collected for routine health assessments. The farmers involved in the research were informed and provided consent to use the animals in the present study. The biological material was provided by Lebanese Health Veterinary Service.
Informed Consent Statement
Not applicable.
Data Availability Statement
The data presented in this study are available on request from the corresponding author. The data are not publicly available to preserve privacy of the data.
Acknowledgments
We are grateful to the Lebanese sheep farmers for their support in the research and to the Lebanese veterinarians for their assistance in the animal care.
Conflicts of Interest
The authors declare no conflict of interest.
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Table 1.
Number and ID of single nucleotide polymorphisms (SNPs), genotype, allele frequency, Hardy–Weinberg equilibrium, locus, and amino acid (AA) change in the MTNR1A gene. The sequence is in a reverse orientation on the genome, and the SNPs are ordered according to their positions in the latest sheep genome version (Oar_Rambouillet_v1.0, GCF_002742125.1).
Table 1.
Number and ID of single nucleotide polymorphisms (SNPs), genotype, allele frequency, Hardy–Weinberg equilibrium, locus, and amino acid (AA) change in the MTNR1A gene. The sequence is in a reverse orientation on the genome, and the SNPs are ordered according to their positions in the latest sheep genome version (Oar_Rambouillet_v1.0, GCF_002742125.1).
| Alias | SNP ID | Position on Oar_rambouillet_v1.0 | Genotype | Genotype Frequency | Allele | Allele Frequency | Hardy–Weinberg | MTNR1A Region | AA Change |
|---|---|---|---|---|---|---|---|---|---|
| SNP1 | rs409468184 | 17379432 | GG | 62.9 | G | 0.815 | 0.023 | Promoter | - |
| GA | 37.1 | A | 0.185 | ||||||
| AA | 0 | ||||||||
| SNP2 | rs428941001 | 17379252 | CC | 61.2 | C | 0.806 | 0.016 | Promoter | - |
| CA | 38.8 | A | 0.194 | ||||||
| AA | 0 | ||||||||
| SNP3 | rs419424336 | 17379237 | GG | 66.6 | G | 0.833 | 0.045 | Promoter | - |
| GA | 33.4 | A | 0.167 | ||||||
| AA | 0 | ||||||||
| SNP4 | rs429917252 | 17379178 | CC | 65.1 | C | 0.825 | 0.035 | Promoter | - |
| CT | 34.9 | T | 0.175 | ||||||
| TT | 0 | ||||||||
| SNP5 | rs405080439 | 17379097 | GG | 61.9 | G | 0.809 | 0.019 | Promoter | - |
| GA | 38.1 | A | 0.191 | ||||||
| AA | 0 | ||||||||
| SNP6 | rs428880789 | 17379083 | GG | 64.8 | G | 0.824 | 0.033 | Promoter | - |
| GA | 35.2 | A | 0.176 | ||||||
| AA | 0 | ||||||||
| SNP7 | rs415456480 | 17379037 | GG | 62.1 | G | 0.811 | 0.019 | Promoter | - |
| GA | 37.9 | A | 0.189 | ||||||
| AA | 0 | ||||||||
| SNP8 | rs406184829 | 17378992 | CC | 0 | C | 0.349 | 0.000 | Promoter | - |
| CT | 69.8 | T | 0.651 | ||||||
| TT | 30.2 | ||||||||
| SNP9 | rs411931887 | 17378874 | CC | 63.0 | C | 0.778 | 0.152 | Promoter | - |
| CT | 29.6 | T | 0.222 | ||||||
| TT | 7.4 | ||||||||
| SNP10 | rs402949406 | 17378871 | CC | 0 | C | 0.175 | 0.035 | Promoter | - |
| CA | 34.9 | A | 0.825 | ||||||
| AA | 65.1 | ||||||||
| SNP11 | rs426266687 | 17378842 | CC | 66.8 | C | 0.834 | 0.047 | Promoter | - |
| CT | 33.2 | T | 0.166 | ||||||
| TT | 0 | ||||||||
| SNP12 | rs399461430 | 17378769 | CC | 0 | C | 0.343 | 0.000 | Promoter | - |
| CT | 68.5 | T | 0.657 | ||||||
| TT | 31.5 | ||||||||
| SNP13 | rs400561563 | 17378728 | CC | 55.5 | C | 0.703 | 0.004 | Promoter | - |
| CT | 29.6 | T | 0.297 | ||||||
| TT | 14.9 | ||||||||
| SNP14 | rs419743392 | 17378706 | GG | 67.9 | G | 0.840 | 0.056 | Promoter | - |
| GA | 32.1 | A | 0.160 | ||||||
| AA | 0 | ||||||||
| SNP15 | rs406334919 | 17378624 | CC | 0 | G | 0.176 | 0.033 | Promoter | - |
| CT | 35.1 | A | 0.824 | ||||||
| TT | 64.9 | ||||||||
| SNP16 | ss213714057 | 17377903 | GG | 66.6 | G | 0.814 | 0.822 | exon 1 | - |
| GA | 29.6 | A | 0.186 | ||||||
| AA | 3.8 | ||||||||
| SNP17 | - | 17377662 | GG | 3.2 | G | 0.187 | 0.854 | intron 1 | - |
| GC | 30.9 | C | 0.813 | ||||||
| CC | 65.9 | ||||||||
| SNP18 | rs419680097 | 17355611 | CC | 48.1 | C | 0.685 | 0.564 | Exon 2 | - |
| CA | 40.7 | A | 0.315 | ||||||
| AA | 11.2 | ||||||||
| SNP19 | rs406779174 | 17355458 | GG | 74.1 | G | 0.852 | 0.231 | Exon 2 | - |
| GA | 22.2 | A | 0.148 | ||||||
| AA | 3.7 | ||||||||
| SNP20 | rs430181568 | 17355452 | CC | 49.2 | C | 0.691 | 0.476 | Exon 2 | - |
| CT | 39.7 | T | 0.309 | ||||||
| TT | 11.1 | ||||||||
| SNP21 | rs407388227 | 17355358 | CC | 49.2 | C | 0.691 | 0.476 | Exon 2 | Ile/Val |
| CT | 39.7 | T | 0.309 | ||||||
| TT | 11.1 | ||||||||
| SNP22 | rs404378206 | 17355190 | CC | 92.5 | C | 0.963 | 0.697 | Exon 2 | Ile/Val |
| CT | 7.5 | T | 0.037 | ||||||
| TT | 0 | ||||||||
| SNP23 | rs429718221 | 17355173 | GG | 44.4 | G | 0.666 | 0.984 | Exon 2 | - |
| GA | 44.4 | A | 0.334 | ||||||
| AA | 11.2 | ||||||||
| SNP24 | rs403212791 | 17354971 | GG | 73.0 | G | 0.865 | 0.119 | Exon 2 | Cys/Arg |
| GA | 27.0 | A | 0.135 | ||||||
| AA | 0 | ||||||||
| SNP25 | rs426523476 | 17354963 | GG | 50.1 | G | 0.702 | 0.695 | Exon 2 | - |
| GA | 40.2 | A | 0.298 | ||||||
| AA | 9.7 | ||||||||
| SNP26 | rs413084140 | 17354943 | CC | 11.9 | C | 0.335 | 0.761 | Exon 2 | His/Arg |
| CT | 43.2 | T | 0.665 | ||||||
| TT | 44.9 | ||||||||
| SNP27 | rs403826495 | 17354935 | CC | 13.8 | C | 0.344 | 0.384 | Exon 2 | Ile/Val |
| CT | 41.2 | T | 0.656 | ||||||
| TT | 45.0 | ||||||||
| SNP28 | rs423194759 | 17354883 | CC | 41.3 | C | 0.661 | 0.272 | 3′Utr | - |
| CT | 49.7 | T | 0.339 | ||||||
| TT | 9.0 | ||||||||
| SNP29 | rs414185743 | 17354835 | CC | 14.2 | C | 0.370 | 0.827 | 3′Utr | - |
| CT | 45.6 | T | 0.630 | ||||||
| TT | 40.2 | ||||||||
| SNP30 | rs400830807 | 17354827 | GG | 74.2 | G | 0.871 | 0.139 | 3′Utr | - |
| GA | 25.8 | A | 0.129 | ||||||
| AA | 0 | ||||||||
| SNP31 | rs410686330 | 17354746 | GG | 85.3 | C | 0.927 | 0.428 | 3′Utr | - |
| GA | 14.7 | T | 0.073 | ||||||
| AA | 0 |
Table 2.
Litter size, fertility rate, and days to lambing (DTL) for each genotype at SNP20/SNP21. Data are expressed as LSmeans.
Table 2.
Litter size, fertility rate, and days to lambing (DTL) for each genotype at SNP20/SNP21. Data are expressed as LSmeans.
| Genotype | Litter Size | Lambing Rate (%) | DTL |
|---|---|---|---|
| C/C | 1.2 | 88 | 164 ± 18.1 a |
| C/T | 1.1 | 87 | 170 ± 18.2 a |
| T/T | 1.1 | 87 | 184 ± 22.4 b |
Note: DTL = days to lambing; Different lower-case letters (a, b) indicate differences for p ≤ 0.05.
Table 3.
Haplotypes and their frequency in the enrolled ewes.
| Haplocode | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 | 19 | 20 | 21 | 22 | 23 | 24 | 25 | 26 | 27 | 28 | 29 | 30 | 31 | Haplotype Frequency |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | A | A | A | T | A | A | A | C | T | C | T | C | C | A | C | A | G | A | G | T | T | C | A | G | A | C | C | T | C | G | A | 0.05470 |
| 2 | A | A | A | T | A | A | A | C | T | C | T | C | C | A | C | A | G | C | A | C | C | C | G | A | G | T | T | C | C | A | G | 0.05470 |
| 3 | G | C | G | C | G | G | G | T | C | A | C | T | C | G | T | G | C | C | G | C | C | C | G | G | G | T | T | C | C | G | G | 0.27695 |
| 4 | G | C | G | C | G | G | G | T | C | A | C | T | C | G | T | G | C | C | G | C | C | C | G | G | G | T | T | C | T | G | G | 0.14733 |
| 5 | G | C | G | C | G | G | G | T | C | A | C | T | T | G | T | G | C | A | G | T | T | C | A | G | A | C | C | T | C | G | G | 0.20156 |
Table 4.
Litter size, fertility rate, and DTL according to haplotypes. Data are expressed as LSmeans.
Table 4.
Litter size, fertility rate, and DTL according to haplotypes. Data are expressed as LSmeans.
| Haplocode | Litter Size | Fertility Rate (%) | DTL |
|---|---|---|---|
| 1 | 1.1 | 82 | 183 ± 22.6 b |
| 2 | 1.0 | 84 | 166 ± 18.3 a |
| 3 | 1.1 | 87 | 161 ± 18.2 a |
| 4 | 1.0 | 88 | 167 ± 19.1 a |
| 5 | 1.0 | 81 | 182 ± 20.4 b |
Note: DTL = days to lambing; Different lower-case letters (a, b) indicate differences for p ≤ 0.05.
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Cosso, G.; Nehme, M.; Luridiana, S.; Pulinas, L.; Curone, G.; Hosri, C.; Carcangiu, V.; Mura, M.C. Detection of Polymorphisms in the MTNR1A Gene and Their Association with Reproductive Performance in Awassi Ewes. Animals 2021, 11, 583. https://doi.org/10.3390/ani11020583
AMA Style
Cosso G, Nehme M, Luridiana S, Pulinas L, Curone G, Hosri C, Carcangiu V, Mura MC. Detection of Polymorphisms in the MTNR1A Gene and Their Association with Reproductive Performance in Awassi Ewes. Animals. 2021; 11(2):583. https://doi.org/10.3390/ani11020583
Chicago/Turabian StyleCosso, Giovanni, Michella Nehme, Sebastiano Luridiana, Luisa Pulinas, Giulio Curone, Chadi Hosri, Vincenzo Carcangiu, and Maria Consuelo Mura. 2021. "Detection of Polymorphisms in the MTNR1A Gene and Their Association with Reproductive Performance in Awassi Ewes" Animals 11, no. 2: 583. https://doi.org/10.3390/ani11020583
APA StyleCosso, G., Nehme, M., Luridiana, S., Pulinas, L., Curone, G., Hosri, C., Carcangiu, V., & Mura, M. C. (2021). Detection of Polymorphisms in the MTNR1A Gene and Their Association with Reproductive Performance in Awassi Ewes. Animals, 11(2), 583. https://doi.org/10.3390/ani11020583
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