# Identification of genomic characteristics and selective signals in Guizhou black goat

**Authors:** Lingle Chang, Yundi Zheng, Sheng Li, Xi Niu, Shihui Huang, Qingmeng Long, Xueqin Ran, Jiafu Wang

PMC · DOI: 10.1186/s12864-023-09954-6 · 2024-02-09

## TL;DR

This study identifies genetic traits and selection signals in Guizhou black goats, revealing genes linked to meat quality, cold resistance, and reproduction.

## Contribution

The study provides new insights into the genomic diversity and selection signatures unique to Guizhou black goats.

## Key findings

- Guizhou black goats show high genetic diversity and low linkage disequilibrium compared to other goat breeds.
- Candidate genes related to meat quality, cold resistance, and reproduction were identified.
- Selection signatures were found in genomic regions associated with growth, disease resistance, and fertility.

## Abstract

Guizhou black goat is one of the indigenous black goat breeds in the southwest region of Guizhou, China, which is an ordinary goat for mutton production. They are characterized by moderate body size, black coat, favorite meat quality with tender meat and lower odor, and tolerance for cold and crude feed. However, little is known about the genetic characteristics or variations underlying their important economic traits.

Here, we resequenced the whole genome of Guizhou black goat from 30 unrelated individuals breeding in the five core farms. A total of 9,835,610 SNPs were detected, and 2,178,818 SNPs were identified specifically in this breed. The population structure analysis revealed that Guizhou black goat shared a common ancestry with Shaanbei white cashmere goat (0.146), Yunshang black goat (0.103), Iran indigenous goat (0.054), and Moroccan goat (0.002). However, Guizhou black goat showed relatively higher genetic diversity and a lower level of linkage disequilibrium than the other seven goat breeds by the analysis of the nucleotide diversity, linkage disequilibrium decay, and runs of homozygosity. Based on FST and θπ values, we identified 645, 813, and 804 selected regions between Guizhou black goat and Yunshang black goat, Iran indigenous goat, and cashmere goats. Combined with the results of XP-EHH, there were 286, 322, and 359 candidate genes, respectively. Functional annotation analysis revealed that these genes are potentially responsible for the immune response (e.g., CD28, CD274, IL1A, TLR2, and SLC25A31), humility-cold resistance (e.g., HBEGF, SOSTDC1, ARNT, COL4A1/2, and EP300), meat quality traits (e.g., CHUK, GAB2, PLAAT3, and EP300), growth (e.g., GAB2, DPYD, and CSF1), fertility (e.g., METTL15 and MEI1), and visual function (e.g., PANK2 and NMNAT2) in Guizhou black goat.

Our results indicated that Guizhou black goat had a high level of genomic diversity and a low level of linkage disequilibrium in the whole genome. Selection signatures were detected in the genomic regions that were mainly related to growth and development, meat quality, reproduction, disease resistance, and humidity-cold resistance in Guizhou black goat. These results would provide a basis for further resource protection and breeding improvement of this very local breed.

The online version contains supplementary material available at 10.1186/s12864-023-09954-6.

## Linked entities

- **Genes:** CD28 (CD28 molecule) [NCBI Gene 940], CD274 (CD274 molecule) [NCBI Gene 29126], IL1A (interleukin 1 alpha) [NCBI Gene 3552], TLR2 (toll like receptor 2) [NCBI Gene 7097], SLC25A31 (solute carrier family 25 member 31) [NCBI Gene 83447], HBEGF (heparin binding EGF like growth factor) [NCBI Gene 1839], SOSTDC1 (sclerostin domain containing 1) [NCBI Gene 25928], ARNT (aryl hydrocarbon receptor nuclear translocator) [NCBI Gene 405], COL4A1 (collagen type IV alpha 1 chain) [NCBI Gene 1282], COL4A2 (collagen type IV alpha 2 chain) [NCBI Gene 1284], EP300 (EP300 lysine acetyltransferase) [NCBI Gene 2033], CHUK (component of inhibitor of nuclear factor kappa B kinase complex) [NCBI Gene 1147], GAB2 (GRB2 associated binding protein 2) [NCBI Gene 9846], PLAAT3 (phospholipase A and acyltransferase 3) [NCBI Gene 11145], DPYD (dihydropyrimidine dehydrogenase) [NCBI Gene 1806], CSF1 (colony stimulating factor 1) [NCBI Gene 1435], METTL15 (methyltransferase 15, mitochondrial 12S rRNA N4-cytidine) [NCBI Gene 196074], MEI1 (meiotic double-stranded break formation protein 1) [NCBI Gene 150365], PANK2 (pantothenate kinase 2) [NCBI Gene 80025], NMNAT2 (nicotinamide nucleotide adenylyltransferase 2) [NCBI Gene 23057]

## Full-text entities

- **Genes:** SOSTDC1 [NCBI Gene 102178138], METTL15 [NCBI Gene 102181700], GAB2 [NCBI Gene 102177137], NMNAT2 [NCBI Gene 102170807], HBEGF [NCBI Gene 102185462], TLR2 [NCBI Gene 100860747], CSF1 [NCBI Gene 102185051], MEI1 [NCBI Gene 102169168], IL1A [NCBI Gene 100861289], SLC25A31 [NCBI Gene 102176546], DPYD [NCBI Gene 102181553], ARNT [NCBI Gene 102183027], EP300 [NCBI Gene 102187383], CD28 [NCBI Gene 102179142], CD274 [NCBI Gene 102179284], CHUK [NCBI Gene 102181262], PANK2 [NCBI Gene 102177992]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10854126/full.md

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Source: https://tomesphere.com/paper/PMC10854126