RNA-mediated epigenetic regulation of DNA copy number

被引:53
|
作者
Nowacki, Mariusz [1 ,2 ]
Haye, Joanna E. [1 ]
Fang, Wenwen [1 ]
Vijayan, Vikram [1 ,3 ]
Landweber, Laura F. [1 ]
机构
[1] Princeton Univ, Dept Ecol & Evolutionary Biol, Princeton, NJ 08544 USA
[2] Univ Bern, Inst Cell Biol, CH-3012 Bern, Switzerland
[3] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
copy number variation; genome rearrangement; COMPARATIVE GENOMIC HYBRIDIZATION; MICROARRAY ANALYSIS; POLYMORPHISM; REARRANGEMENTS; REVEALS; GENES; OVERAMPLIFICATION; AMPLIFICATION; DUPLICATIONS; MOLECULES;
D O I
10.1073/pnas.1012236107
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
Increasing evidence suggests that parentally supplied RNA plays crucial roles during eukaryotic development. This epigenetic contribution may regulate gene expression from the earliest stages. Although present in a variety of eukaryotes, maternally inherited characters are especially prominent in ciliated protozoa, in which parental noncoding RNA molecules instruct whole-genome reorganization. This includes removal of nearly all noncoding DNA and sorting the remaining fragments, producing extremely gene-rich somatic genomes. Chromosome fragmentation and extensive replication produce variable DNA copy numbers in the somatic genome. Understanding the forces that drive and regulate copy number change is fundamental. We show that RNA molecules present in parental cells during sexual reproduction can regulate chromosome copy number in the developing nucleus of the ciliate Oxytricha. Experimentally induced changes in RNA abundance can both increase and decrease the levels of corresponding DNA molecules in progeny, demonstrating epigenetic inheritance of chromosome copy number. These results suggest that maternal RNA, in addition to controlling gene expression or DNA processing, can also program DNA amplification levels.
引用
收藏
页码:22140 / 22144
页数:5
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