Making a long story short: noncoding RNAs and chromosome change

被引:27
作者
Brown, J. D. [1 ,2 ]
Mitchell, S. E. [1 ]
O'Neill, R. J. [1 ]
机构
[1] Univ Connecticut, Dept Mol & Cell Biol, Storrs, CT 06269 USA
[2] Univ Connecticut, Allied Hlth Sci Dept, Storrs, CT USA
基金
美国国家科学基金会;
关键词
non-coding; ncRNA; small RNA; chromosome; evolution; karyotype; FRAGILE SITES; FUNCTIONAL ELEMENTS; BREAKPOINT REUSE; TINY RNAS; CENTROMERE; REPLICATION; GENOME; TRANSCRIPTION; EVOLUTION; HETEROCHROMATIN;
D O I
10.1038/hdy.2011.104
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071301 [植物生态学];
摘要
As important as the events that influence selection for specific chromosome types in the derivation of novel karyotypes, are the events that initiate the changes in chromosome number and structure between species, and likewise polymorphisms, variants and disease states within species. Although once thought of as transcriptional 'noise', noncoding RNAs (ncRNAs) are now recognized as important mediators of epigenetic regulation and chromosome stability. Here we highlight recent work that illustrates the influence short and long ncRNAs have as participants in the function and stability of chromosome regions such as centromeres, telomeres, evolutionary breakpoints and fragile sites. We summarize recent evidence that ncRNAs can facilitate chromosome change and present mechanisms by which ncRNAs create DNA breaks. Finally, we present hypotheses on how they may create novel karyotypes and thus affect chromosome evolution. Heredity (2012) 108, 42-49; doi:10.1038/hdy.2011.104; published online 9 November 2011
引用
收藏
页码:42 / 49
页数:8
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