Sensitive high-throughput single-cell RNA-seq reveals within-clonal transcript correlations in yeast populations
文献类型:期刊论文
作者 | Nadal-Ribelles, Mariona1,2,3,6; Islam, Saiful1,2; Wei, Wu1,2; Nguyen, Michelle1,2; Steinmetz, Lars M.1,2; Latorre, Pablo3,6; de Nadal, Eulalia3,6; Posas, Francesc3,6; Wei, Wu4; Steinmetz, Lars M.5 |
刊名 | NATURE MICROBIOLOGY |
出版日期 | 2019 |
卷号 | 4期号:4页码:683-692 |
ISSN号 | 2058-5276 |
DOI | 10.1038/s41564-018-0346-9 |
文献子类 | Article |
英文摘要 | Single-cell RNA sequencing has revealed extensive cellular heterogeneity within many organisms, but few methods have been developed for microbial clonal populations. The yeast genome displays unusually dense transcript spacing, with interleaved and overlapping transcription from both strands, resulting in a minuscule but complex pool of RNA that is protected by a resilient cell wall. Here, we have developed a sensitive, scalable and inexpensive yeast single-cell RNA-seq (yscRNA-seq) method that digitally counts transcript start sites in a strand- and isoform-specific manner. YscRNA-seq detects the expression of low-abundance, noncoding RNAs and at least half of the protein-coding genome in each cell. In clonal cells, we observed a negative correlation for the expression of sense-antisense pairs, whereas paralogs and divergent transcripts co-expressed. By combining yscRNA-seq with index sorting, we uncovered a linear relationship between cell size and RNA content. Although we detected an average of -3.5 molecules per gene, the number of expressed isoforms is restricted at the single-cell level. Remarkably, the expression of metabolic genes is highly variable, whereas their stochastic expression primes cells for increased fitness towards the corresponding environmental challenge. These findings suggest that functional transcript diversity acts as a mechanism that provides a selective advantage to individual cells within otherwise transcriptionally heterogeneous populations. |
学科主题 | Microbiology |
WOS关键词 | SACCHAROMYCES-CEREVISIAE ; GENES ; CYCLE ; PCR ; QUANTIFICATION ; IDENTIFICATION ; VALIDATION ; NOISE ; START |
语种 | 英语 |
出版者 | NATURE PUBLISHING GROUP |
WOS记录号 | WOS:000461999200021 |
版本 | 出版稿 |
源URL | [http://202.127.25.144/handle/331004/483] |
专题 | 中国科学院上海生命科学研究院营养科学研究所 |
作者单位 | 1.Stanford Univ, Stanford Genome Technol Ctr, Stanford, CA 94305 USA; 2.Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA; 3.Barcelona Inst Sci & Technol, Cell Signaling, Inst Res Biomed, Barcelona, Spain; 4.Univ Chinese Acad Sci, Chinese Acad Sci, CAS Key Lab Computat Biol,Shanghai Inst Biol Sci, CAS MPG Partner Inst Computat Biol,Shanghai Inst, Shanghai, Peoples R China; 5.Genome Biol Unit, European Mol Biol Lab, Heidelberg, Germany, 6.Univ Pompeu Fabra, Cell Signaling Res Grp, Dept Ciencies Expt & Salut, Barcelona, Spain; |
推荐引用方式 GB/T 7714 | Nadal-Ribelles, Mariona,Islam, Saiful,Wei, Wu,et al. Sensitive high-throughput single-cell RNA-seq reveals within-clonal transcript correlations in yeast populations[J]. NATURE MICROBIOLOGY,2019,4(4):683-692. |
APA | Nadal-Ribelles, Mariona.,Islam, Saiful.,Wei, Wu.,Nguyen, Michelle.,Steinmetz, Lars M..,...&Steinmetz, Lars M..(2019).Sensitive high-throughput single-cell RNA-seq reveals within-clonal transcript correlations in yeast populations.NATURE MICROBIOLOGY,4(4),683-692. |
MLA | Nadal-Ribelles, Mariona,et al."Sensitive high-throughput single-cell RNA-seq reveals within-clonal transcript correlations in yeast populations".NATURE MICROBIOLOGY 4.4(2019):683-692. |
入库方式: OAI收割
来源:上海营养与健康研究所
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