首页|四倍体油茶全基因组SSR位点开发与特征分析

四倍体油茶全基因组SSR位点开发与特征分析

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[目的]传统的油茶育种工作效率低、周期长,分子标记辅助育种已成为推动油茶遗传改良的必要方法,对油茶基因组SSR位点进行整体统计分析,为提高油茶的选育效果、缩短选育周期提供了一条有效途径。通过对四倍体油茶基因组SSR位点进行搜索,统计分析其基因组SSR序列的分布模式及特征,获得优质、有价值的SSR分子标记位点,为进一步开展油茶品种的遗传分析、分子标记辅助育种、指纹鉴定等研究工作提供便利条件。[方法]本研究基于已获得的四倍体油茶全基因组数据,使用MISA软件全面搜索基因组中 1~6核苷酸各重复类型的SSR位点,统计分析其分布模式及特征,通过Primer3。0 软件进行批量SSR引物设计。[结果]在全长为11 069 152 038 bp的四倍体油茶全基因组中共搜索到不同类型SSR位点6 254 681个,一共鉴定出 463 个不同重复基元,平均 1。77 kb出现一个SSR位点;出现频率最高的是单核苷酸重复类型SSR位点,占比 62。08%,六核苷酸重复类型SSR位点数量最少,仅占比 0。46%;在四倍体油茶基因组SSR序列中A、T碱基占据绝对优势,而G、C含量较少,具有碱基偏好性。四倍体油茶基因组各类型SSR序列的整体长度区间为10~187 bp,平均长度 15。57 bp;除单核苷酸重复类型,长度≥20 bp的SSR序列占全部SSR序列的15。75%,其中二、三、四核苷酸三种重复类型SSR长度变异程度显著高于五、六核苷酸重复类型,因此,二、三、四核苷酸重复类型为设计SSR引物的主要标记来源;基于四倍体油茶基因组SSR位点数据,共开发引物1 358 248对。[结论]本研究首次对四倍体油茶全基因组中SSR位点的分布模式与特征进行整体统计分析,并批量开发SSR引物,为油茶分子标记辅助育种提供参考。
Development and characterization of whole genome SSR in tetraploid Camellia oleifera
[Objective]Traditional breeding of Camellia oleifera has low efficiency and long cycle,and molecular marker-assisted breeding has become a necessary method to promote the genetic improvement.The overall statistical analysis of the SSR loci of genome provides an effective vehicle,which help to improve the breeding effect and shorten the breeding cycle of C.oleifera.Obtaining high-quality and valuable SSR molecular marker loci by searching and analyzing the distribution pattern and characteristics of SSR loci of tetraploid C.oleifera genome can provide convenient conditions for further research on genetic analysis,molecular marker assisted breeding and fingerprint identification.[Method]Based on the whole genome data of tetraploid C.oleifera,the SSR loci of 1-6 nucleotide repeat types were searched comprehensively and the distribution pattern and characteristics of types of SSR were counted by MISA.SSR primers were designed by Primer 3.0 software.[Result]A total of 6 254 681 SSR loci of different types were found in the whole genome of tetraploid C.oleifera with a total length of 11 069 152 038 bp,and 463 different repeats were identified,a SSR locus appeared at 1.77 kb on average.SSR sites of single nucleotide repeat type were the most,accounting for 62.08%,while SSR sites of hexanucleotide repeat type were the least,accounting for only 0.46%.A and T bases were dominant in SSR sequences of tetraploid C.oleifera genome,while G and C were less in content and have base preference.The SSR sequence length of tetraploid C.oleifera genome ranged from 10 to 187 bp,with an average length of 15.57 bp.Except for single nucleotide repeat types,the SSR sequences with sequence length≥20 bp accounted for 15.75%of all SSR sequences,the SSR length variation of dinucleotide,trinucleotide and tetranucleotide repeats was significantly higher than that of pentanucleotide and hexanucleotide,dinucleotide,trinucleotide and tetranucleotide repeats were the main marker sources for designing SSR primers.Based on the SSR loci mining of tetraploid C.oleifera genome,1 358 248 pairs of primers were developed.[Conclusion]This study is the first attempt to conduct overall statistical analysis on the distribution pattern and characteristics of SSR loci and develop SSR primers in the whole genome of tetraploid C.oleifera,which will provide reference for molecular marker-assisted breeding of C.oleifera.

tetraploid Camellia oleiferagenomeSSRnucleotide

童海浪、张华健、李健、邓红达、韩志强

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中南林业科技大学 林木遗传育种实验室,湖南 长沙 410004

四倍体油茶 基因组 SSR 核苷酸

湖南省林业科技创新项目湖南省研究生科技创新项目中南林业科技大学研究生科技创新基金

XLK202101-2CX202207132022CX02011

2024

中南林业科技大学学报
中南林业科技大学

中南林业科技大学学报

CSTPCD北大核心
影响因子:1.442
ISSN:1673-923X
年,卷(期):2024.44(3)
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