Exploration of Genetic Variations through Single-cell Whole-genome Sequencing in the Model Ciliate Tetrahymena thermophila

被引:9
|
作者
Chen, Kai [1 ,2 ]
Wang, Guangying [1 ]
Xiong, Jie [1 ]
Jiang, Chuanqi [1 ]
Miao, Wei [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Inst Hydrobiol, Key Lab Aquat Biodivers & Conservat, Wuhan 430072, Hubei, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Wuhan 430072, Hubei, Peoples R China
[4] CAS Ctr Excellence Anim Evolut & Genet, Kunming 650223, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
Ciliated protozoa; population genetics; single-cell resequencing; variation detection; whole-genome amplification; DNA; AMPLIFICATION; NUCLEOTIDE; MUTATION;
D O I
10.1111/jeu.12746
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Ciliates are unicellular eukaryotes with separate germline and somatic genomes and diverse life cycles, which make them a unique model to improve our understanding of population genetics through the detection of genetic variations. However, traditional sequencing methods cannot be directly applied to ciliates because the majority are uncultivated. Single-cell whole-genome sequencing (WGS) is a powerful tool for studying genetic variation in microbes, but no studies have been performed in ciliates. We compared the use of single-cell WGS and bulk DNA WGS to detect genetic variation, specifically single nucleotide polymorphisms (SNPs), in the model ciliate Tetrahymena thermophila. Our analyses showed that (i) single-cell WGS has excellent performance regarding mapping rate and genome coverage but lower sequencing uniformity compared with bulk DNA WGS due to amplification bias (which was reproducible); (ii) false-positive SNP sites detected by single-cell WGS tend to occur in genomic regions with particularly high sequencing depth and high rate of C:G to T:A base changes; (iii) SNPs detected in three or more cells should be reliable (an detection efficiency of 83.4-97.4% was obtained for combined data from three cells). This analytical method could be adapted to measure genetic variation in other ciliates and broaden research into ciliate population genetics.
引用
收藏
页码:954 / 965
页数:12
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