Abstract

Simple SummaryIncreasing litter size is critical for the intensive sheep production system. Genetic marker-assisted selection (MAS) based on proven molecular indicators could enhance the efficacy of sheep selection with improving litter size traits. Many single nucleotide polymorphisms (SNPs) linked with litter size in Hu sheep and Small-tailed Han sheep have been identified. However, they usually explain a small portion of genetic variation and additional genetic markers linked with litter size have not been found. The present study investigated the potential SNPs in ten genes as candidate markers for improved litter size in sheep. As a result, nine SNPs in six out of ten genes can be served as useful genetic markers to improve the selection of litter size since they are significantly associated with litter size either in Hu sheep or Small-tailed Han sheep. Further, a combined haplotypes analysis of the two loci (LIFR: g.35862868C>T and LIFR: g.35862947G>T) revealed that H2H3 (CTTT) combined haplotypes had the largest litter size than the rest combined haplotypes and more than those with either mutation alone in Small-tailed Han sheep. Our knowledge is essential to implement the MAS in sheep and further to increase the profitability in the sheep industry.Hu sheep and Small-tailed Han sheep are the most widely raised and most famous maternal sheep breeds in China, which are known for precocious puberty, perennial oestrus and high fecundity (1–6 lambs each parity). Therefore, it is crucial to increase litter size of these two breeds for intensive sheep industry. The objective of this study was to identify potential genetic markers linked with sheep litter size located at ten genes. This study collected blood sample of 537 Hu sheep and 420 Small-tailed Han sheep with litter size of first parity. The average litter sizes in Hu sheep and Small-tailed Han sheep were 2.21 and 1.93. DNA-pooling sequencing method was used for detecting the potential single nucleotide polymorphisms (SNPs) in ten genes related to follicle development and female reproduction. SNPscan® was used for individually genotyping. As a result, a total of 78 putative SNPs in nine out of ten candidate genes (except NOG) were identified. In total, 50 SNPs were successfully genotyped in Hu sheep and Small-tailed Han sheep. After quality control, a total of 42 SNPs in Hu sheep and 44 SNPs in Small-tailed Han sheep were finally used for further analysis. Association analysis revealed that nine SNPs within six genes (KIT: g.70199073A>G, KITLG: g.124520653G>C, ADAMTS1: g.127753565T>C, ADAMTS1: g.127754640G>T, NCOA1: g.31928165C>T, NCOA1: g.32140565G>A, LIFR: g.35862868C>T, LIFR: g.35862947G>T and NGF: g.91795933T>C) were significantly associated with litter size in Hu sheep or Small-tailed Han sheep. A combined haplotypes analysis of the two loci (LIFR: g.35862868C>T and LIFR: g.35862947G>T) revealed that H2H3 (CTTT) combined haplotypes had the largest litter size than the rest combined haplotypes and more than those with either mutation alone in Small-tailed Han sheep. Taken together, our study suggests that nine significant SNPs in six genes can be served as useful genetic markers for MAS in sheep.

Highlights

  • Litter size is one of the most important economic traits because it has a noticeable impact

  • The genotypic correlation coefficient of three pairs of technical repeats equal to one and no genotyping signals were detected in two blank samples, indicating that the SNPscan® method is reliable

  • If single nucleotide polymorphisms (SNPs) from the candidate genes were found significantly associated with litter size in a sheep breed, they could be served as molecular indicators for marker-assisted selection (MAS)

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Summary

Objectives

The objective of this study was to identify potential genetic markers linked with sheep litter size located at ten genes. The objectives of this study were to scan SNPs in these ten genes and to investigate the association of SNPs with litter size in Hu sheep (n = 537) and Small-tailed Han sheep (n = 420). The objectives of this study were to scan SNPs in these ten genes and to investigate the association sheep

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