Xia Lunbin, Bi Shaoshuai, Zhang Yafei, Chen Cunwu, Chen Naidong
College of Biological and Pharmaceutical Engineering, West Anhui University, Lu'an, 237012, P.R. China.
Small Animal Diagnosis and Treatment Experimental Training Center, West Anhui University, Lu'an, 237012, P.R. China.
BMC Genom Data. 2025 May 13;26(1):34. doi: 10.1186/s12863-025-01326-1.
The Wan-Xi white goose (WXG), an indigenous Chinese waterfowl (Anserini: Anserinae), is crucial for goose germplasm conservation. This study aimed to sequence and analyze the complete mitochondrial DNA (mtDNA) of WXG using the BGISEQ-500 platform. The mtDNA's structure and function were investigated to gain insights into its genetic diversity and population structure.
The mtDNA was found to be 16,743 bp long and comprised 22 transfer RNA (tRNA) genes, 2 ribosomal RNA genes, a complement of 13 protein-coding genes (PCGs), as well as a single noncoding control region known as the D-loop. Notably, all tRNA genes, except for trnS1-tRNA which lacked the dihydrouridine stem, were predicted to adopt the typical cloverleaf structure. Given the genetic variability across the mtDNA of Anser spp. and the intergenic gaps identified by codon analysis, the codon usage patterns were comprehensively examined via comparative analysis of the mtDNAs of WXG and 24 other Anser spp. The relative synonymous codon usage (RSCU) values of the 13 mitochondrial PCGs of WXG were consistent with those of the mitochondrial PCGs of the 24 other Anser spp. Analysis of the neutrality (GC3-GC12), the effective number of codons (ENCs)-GC3, and parity rule 2-bias plots further revealed that natural selection emerged as the primary factor influencing codon bias in Anser sp. High nucleotide diversity (Pi > 0.02) was observed in several regions, including the D-loop, ATP6, 12S rRNA, ND1, 16S rRNA_ND1, COX2, and ND5. Furthermore, the results of nonsynonymous (Ka)/synonymous (Ks) analysis of the 13 mitochondrial PCGs of the 25 species under Anser revealed that the genes were subject to strong purifying selection. The findings of phylogenetic analysis further revealed that WXG and 10 other members of Anser cygnoides clustered into a single branch to form a monophyletic group.
This research provides valuable insights into the mtDNA of WXG, highlighting its genetic diversity and population structure. The identified mutation hotspots and purifying selection on mitochondrial PCGs suggest potential areas for future research on Anser cygnoides. The findings contribute to our understanding of this rare species and its conservation efforts.
皖西白鹅(WXG)是中国本土水禽(雁形目:雁亚科),对鹅种质资源保护至关重要。本研究旨在利用BGISEQ - 500平台对皖西白鹅的完整线粒体DNA(mtDNA)进行测序和分析。对mtDNA的结构和功能进行了研究,以深入了解其遗传多样性和种群结构。
发现mtDNA长度为16743 bp,包含22个转移RNA(tRNA)基因、2个核糖体RNA基因、13个蛋白质编码基因(PCG)以及一个称为D环的单一非编码控制区。值得注意的是,除了缺少二氢尿苷茎的trnS1 - tRNA外,所有tRNA基因预计都采用典型的三叶草结构。鉴于雁属物种mtDNA的遗传变异性以及通过密码子分析确定的基因间隔,通过对皖西白鹅和其他24种雁属物种的mtDNA进行比较分析,全面研究了密码子使用模式。皖西白鹅13个线粒体PCG的相对同义密码子使用(RSCU)值与其他24种雁属物种的线粒体PCG一致。对中性(GC3 - GC12)、有效密码子数(ENC)- GC3和奇偶规则2 - 偏差图的分析进一步表明,自然选择是影响雁属物种密码子偏好的主要因素。在几个区域观察到高核苷酸多样性(Pi > 0.02),包括D环、ATP6、12S rRNA、ND1、16S rRNA_ND1、COX2和ND5。此外,对雁属下25个物种的13个线粒体PCG的非同义(Ka)/同义(Ks)分析结果表明,这些基因受到强烈的纯化选择。系统发育分析结果进一步表明,皖西白鹅和其他10种鸿雁聚为一个单系分支。
本研究为皖西白鹅的mtDNA提供了有价值的见解,突出了其遗传多样性和种群结构。在线粒体PCG上确定的突变热点和纯化选择为鸿雁未来的研究提供了潜在领域。这些发现有助于我们对这一珍稀物种的理解及其保护工作。