Identification of novel noncoding transcripts in telomerase-negative yeast using RNA-seq

被引:9
|
作者
Niederer, Rachel O. [1 ]
Papadopoulos, Nickolas [2 ]
Zappulla, David C. [1 ]
机构
[1] Johns Hopkins Univ, Dept Biol, Baltimore, MD 21218 USA
[2] Johns Hopkins Sidney Kimmel Comprehens Canc Ctr, Ludwig Ctr Canc Genet & Therapeut, Baltimore, MD 21231 USA
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
美国国家卫生研究院;
关键词
SACCHAROMYCES-CEREVISIAE; EUKARYOTIC TRANSCRIPTOME; PERVASIVE TRANSCRIPTION; MAINTENANCE; REVEALS; PATHWAY; GENE; RAP1; RECOMBINATION; DELETION;
D O I
10.1038/srep19376
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Telomerase is a ribonucleoprotein that maintains the ends of linear chromosomes in most eukaryotes. Loss of telomerase activity results in shortening of telomeric DNA and eventually a specific G2/M cell-cycle arrest known as senescence. In humans, telomere shortening occurs during aging, while inappropriate activation of telomerase is associated with approximately 90% of cancers. Previous studies have identified several classes of noncoding RNAs (ncRNA) also associated with aging-related senescence and cancer, but whether ncRNAs are also involved in short-telomere-induced senescence in yeast is unknown. Here, we report 112 putative novel lncRNAs in the yeast Saccharomyces cerevisiae, 41 of which are only expressed in telomerase-negative yeast. Expression of approximately half of the lncRNAs is strongly correlated with that of adjacent genes, suggesting this subset may influence transcription of neighboring genes. Our results reveal a new potential mechanism governing adaptive changes in senescing and post-senescent survivor yeast cells.
引用
收藏
页数:9
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