A Tunable Mechanism Determines the Duration of the Transgenerational Small RNA Inheritance in C. elegans

被引:107
作者
Houri-Ze'evi, Leah [1 ,2 ]
Korem, Yael [3 ]
Sheftel, Hila [3 ]
Faigenbloom, Lior [1 ,2 ]
Toker, Itai Antoine [1 ,2 ]
Dagan, Yael [1 ,2 ]
Awad, Lama [1 ,2 ]
Degani, Luba [1 ,2 ]
Alon, Uri [3 ]
Rechavi, Oded [1 ,2 ]
机构
[1] Tel Aviv Univ, Wise Fac Life Sci, Dept Neurobiol, IL-6997801 Tel Aviv, Israel
[2] Tel Aviv Univ, Sagol Sch, IL-6997801 Tel Aviv, Israel
[3] Weizmann Inst Sci, Dept Mol Cell Biol, IL-7610001 Rehovot, Israel
基金
欧洲研究理事会;
关键词
DOUBLE-STRANDED-RNA; EPIGENETIC INHERITANCE; GENE-EXPRESSION; GERMLINE; INTERFERENCE; CSR-1; PATHWAY; MEMORY; PIRNAS; METHYLATION;
D O I
10.1016/j.cell.2016.02.057
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In C. elegans, small RNAs enable transmission of epigenetic responses across multiple generations. While RNAi inheritance mechanisms that enable "memorization'' of ancestral responses are being elucidated, the mechanisms that determine the duration of inherited silencing and the ability to forget the inherited epigenetic effects are not known. We now show that exposure to dsRNA activates a feedback loop whereby gene-specific RNAi responses dictate the transgenerational duration of RNAi responses mounted against unrelated genes, elicited separately in previous generations. RNA-sequencing analysis reveals that, aside from silencing of genes with complementary sequences, dsRNA-induced RNAi affects the production of heritable endogenous small RNAs, which regulate the expression of RNAi factors. Manipulating genes in this feedback pathway changes the duration of heritable silencing. Such active control of transgenerational effects could be adaptive, since ancestral responses would be detrimental if the environments of the progeny and the ancestors were different.
引用
收藏
页码:88 / 99
页数:12
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