首页|期刊导航|沈阳农业大学学报|乌牛早茶树叶绿体基因组结构解析和密码子偏好性分析

乌牛早茶树叶绿体基因组结构解析和密码子偏好性分析OA

Structure Characterization and Codon Bias Analysis of Chloroplast Genome of Camellia sinensis cv.Wuniuzao

中文摘要英文摘要

[目的]对乌牛早茶树叶绿体基因组进行组装、注释和分析,揭示其与其他山茶属植物的系统进化关系.[方法]采用DNB-SEQ-T7华大基因测序仪对乌牛早茶树的叶绿体全基因组进行高通量测序.基于测序获得的完整叶绿体基因组序列,运用生物信息学方法系统分析其基因组结构特征,比对其重复序列的分布模式,考察其IR边界的收缩与扩展现象,计算其核苷酸多样性和密码子偏好性,并结合其他62种山茶属植物的叶绿体基因组序列,采用最大似然法(ML)构建系统发育树.[结果]乌牛早茶树的叶绿体基因组全长为157 112 bp,其GC含量为37.29%,呈现出典型的四分体结构特征;通过基因组注释分析,共鉴定出135个编码基因,其中包含90个蛋白质编码基因、37个tRNA基因以及8个rRNA基因;在重复序列分析方面,共检测到53个简单重复序列和48个长重复序列.其中,简单重复序列均为A/T单核苷酸重复;而长重复序列则仅包括正向重复序列和回文重复序列;基因组在编码区高度保守,非编码区的差异较大;相对同义密码子使用度大于1的氨基酸有31个,多以A/U结尾,自然选择是密码子偏好性的主要影响因素;基因组具有14个最优密码子(AAA、AAU、ACU、AGU、AUU、CAA、CGU、CUU、GCU、GUU、UGU、UUA、UUG和UUU);仅有ndhB基因和rps8基因的Ka/Ks 值大于1,受到正选择的作用,其余基因的Ka/Ks 值均小于1,受到纯化选择的作用;系统发育分析结果显示:乌牛早茶树与八仙凤凰单枞茶、雷扣茶凤凰单枞茶的亲缘关系较近;分歧时间估计结果显示:乌牛早茶树是在9.88 MYA与上饶大面白(PP024603)进行分化.[结论]研究结果明晰了乌牛早茶树的叶绿体基因组特征,获得了山茶属物种较为合理的系统发育关系,为山茶属遗传多样性研究、适应性进化机制探讨和种质资源保护等提供了理论依据.

[Objective]The chloroplast genome of Camellia sinensis cv.Wuniuzao was assembled,annotated,and analyzed to reveal its phylogenetic relationships with other Camellia species.[Method]The complete chloroplast genome of Camellia sinensis cv.Wuniuzao was sequenced using the DNBSEQ-T7 high-throughput sequencer from BGI.Based on the obtained chloroplast genome sequences,bioinformatics methods were employed to systematically analyze its genomic structural characteristics,compare the distribution patterns of repetitive sequences,investigate the contraction and expansion phenomena of IR boundaries,calculate nucleotide diversity and codon usage bias.Combined with chloroplast genome sequences from 62 other Camellia species,a phylogenetic tree was constructed using the maximum likelihood(ML)method.[Results]The complete chloroplast genome of Camellia sinensis cv.Wuniuzao tea tree was 157 112 bp in length,with a GC content of 37.29%,exhibiting typical quadripartite structural features;A total of 135 coding genes,including 90 protein-coding genes,37 tRNA genes,and 8 rRNA genes were identified by genomic annotation analysis.In terms of repetitive sequence analysis,53 simple repeats and 48 long repeats were detected.Among these,all simple repeats were A/T single nucleotide repeats,while long repeats consisted solely of direct repeats and palindromic repeats.The genome was highly conserved in the coding region,with significant differences in non-coding regions.There were 31 amino acids with relative synonymous codon usage greater than 1,mostly ending in A/U.Natural selection was the main factor affecting codon usage bias.The genome had 14 optimal codons(AAA,AAU,ACU,AGU,AUU,CAA,CGU,CUU,GCU,GUU,UGU,UUA,UUG,and UUU);Only the ndhB gene and rps8 gene had Ka/Ks values greater than 1,indicating positive selection,while the other genes had Ka/Ks values less than 1,indicating purification selection.The results of phylogenetic analysis showed that Camellia sinensis cv.Wuniuzao was closely related to Camellia sinensis cv.Baxian Fenghuang Dancong and Camellia sinensis isolate Leikouchai cultivar Fenghuang Dancong.The estimation of divergence time showed that Camellia sinensis cv.Wuniuzao tea tree differentiated from Camellia sinensis cv.Damianbai from Shangrao(PP024603)at 9.88 MYA.[Conclusion]The research results clarified the chloroplast genome characteristics of Camellia sinensis cv.Wuniuzao tea tree and obtained a relatively reasonable phylogenetic relationship of Camellia species,providing a theoretical basis for genetic diversity research,adaptive evolution mechanism exploration,and germplasm resource protection of Camellia.

尹明华;胡丹;黄佳;邓芸;樊美怡;林月红

上饶师范学院 生命科学学院,江西 上饶 334001上饶师范学院 生命科学学院,江西 上饶 334001上饶师范学院 生命科学学院,江西 上饶 334001上饶师范学院 生命科学学院,江西 上饶 334001上饶师范学院 生命科学学院,江西 上饶 334001上饶师范学院 生命科学学院,江西 上饶 334001

农业科技

乌牛早茶树叶绿体基因组结构解析密码子偏好性系统发育

Camellia sinensis cv.Wuniuzao tea treechloroplast genomestructure analysiscodon biasphylogeny

《沈阳农业大学学报》 2026 (2)

84-96,13

国家自然科学基金项目(31860084,31960079,32060092)江西省科技厅重点研发项目(20192BBF60006,20192BBGL70050,20202BBF63001,20202BBG73010)

10.3969/j.issn.1000-1700.2026.02.010

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