4.7 Article

Genome-wide detection of genetic structure and runs of homozygosity analysis in Anhui indigenous and Western commercial pig breeds using PorcineSNP80k data

Journal

BMC GENOMICS
Volume 23, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12864-022-08583-9

Keywords

Anhui indigenous pig breeds; genetic structure; runs of homozygosity; Inbreeding coefficient; ROH island

Funding

  1. Anhui Academy of Agricultural Sciences Key Laboratory Project [2021YL023]
  2. 68th China Postdoctoral Science Foundation Project [2020M681977]
  3. 2020 Anhui Postdoctoral Research Project [2020A394]
  4. Anhui Natural Science Foundation [2008085QC138, 2108085QC135]
  5. Anhui Swine Industry Technology System Project [AHCYTX-05-15]
  6. Anhui Province Financial Modern Seed Industry Development Fund Project

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This study systematically investigated the population genetic structure of five Anhui indigenous pig breeds and compared them to five Western commercial pig breeds. The occurrence and distribution of ROHs in these breeds were examined, and candidate genes associated with economically important traits were identified. The findings provide valuable insights for the selection and breeding of pig breeds.
Background Runs of homozygosity (ROH) are continuous homozygous regions typically located in the DNA sequence of diploid organisms. Identifications of ROH that lead to reduced performance can provide valuable insight into the genetic architecture of complex traits. Here, we systematically investigated the population genetic structure of five Anhui indigenous pig breeds (AHIPs), and compared them to those of five Western commercial pig breeds (WECPs). Furthermore, we examined the occurrence and distribution of ROHs in the five AHIPs and estimated the inbreeding coefficients based on the ROHs (F-ROH) and homozygosity (F-HOM). Finally, we identified genomic regions with high frequencies of ROHs and annotated candidate genes contained therein. Results The WECPs and AHIPs were clearly differentiated into two separate clades consistent with their geographical origins, as revealed by the population structure and principal component analysis. We identified 13,530 ROHs across all individuals, of which 4,555 and 8,975 ROHs were unique to AHIPs and WECPs, respectively. Most ROHs identified in our study were short (< 10 Mb) or medium (10-20 Mb) in length. WECPs had significantly higher numbers of short ROHs, and AHIPs generally had longer ROHs. F-ROH values were significantly lower in AHIPs than in WECPs, indicating that breed improvement and conservation programmes were successful in AHIPs. On average, F-ROH and F-HOM values were highly correlated (0.952-0.991) in AHIPs and WECPs. A total of 27 regions had a high frequency of ROHs and contained 17 key candidate genes associated with economically important traits in pigs. Among these, nine candidate genes (CCNT2, EGR2, MYL3, CDH13, PROX1, FLVCR1, SETD2, FGF18, and FGF20) found in WECPs were related to muscular and skeletal development, whereas eight candidate genes (CSN1S1, SULT1E1, TJP1, ZNF366, LIPC, MCEE, STAP1, and DUSP) found in AHIPs were associated with health, reproduction, and fatness traits. Conclusion Our findings provide a useful reference for the selection and assortative mating of pig breeds, laying the groundwork for future research on the population genetic structures of AHIPs, ultimately helping protect these local varieties.

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