Hamster PIWI proteins bind to piRNAs with stage-specific size variations during oocyte maturation.
Hamster PIWI proteins bind to piRNAs with stage-specific size variations during oocyte maturation.
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DOI:
10.1093/nar/gkab059
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发表时间:
2021-03-18
影响因子:
14.9
通讯作者:
Siomi H
中科院分区:
文献类型:
--
作者:
Ishino K;Hasuwa H;Yoshimura J;Iwasaki YW;Nishihara H;Seki NM;Hirano T;Tsuchiya M;Ishizaki H;Masuda H;Kuramoto T;Saito K;Sakakibara Y;Toyoda A;Itoh T;Siomi MC;Morishita S;Siomi H
In animal gonads, transposable elements are actively repressed to preserve genome integrity through the PIWI-interacting RNA (piRNA) pathway. In mice, piRNAs are abundantly expressed in male germ cells, and form effector complexes with three distinct PIWIs. The depletion of individual Piwi genes causes male-specific sterility with no discernible phenotype in female mice. Unlike mice, most other mammals have four PIWI genes, some of which are expressed in the ovary. Here, purification of PIWI complexes from oocytes of the golden hamster revealed that the size of the PIWIL1-associated piRNAs changed during oocyte maturation. In contrast, PIWIL3, an ovary-specific PIWI in most mammals, associates with short piRNAs only in metaphase II oocytes, which coincides with intense phosphorylation of the protein. An improved high-quality genome assembly and annotation revealed that PIWIL1- and PIWIL3-associated piRNAs appear to share the 5′-ends of common piRNA precursors and are mostly derived from unannotated sequences with a diminished contribution from TE-derived sequences, most of which correspond to endogenous retroviruses. Our findings show the complex and dynamic nature of biogenesis of piRNAs in hamster oocytes, and together with the new genome sequence generated, serve as the foundation for developing useful models to study the piRNA pathway in mammalian oocytes.
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DOI:
10.1261/rna.045310.114
发表时间:
2014-08
期刊:
RNA (New York, N.Y.)
影响因子:
--
作者:
Hirano T;Iwasaki YW;Lin ZY;Imamura M;Seki NM;Sasaki E;Saito K;Okano H;Siomi MC;Siomi H
通讯作者:
Siomi H
影响因子:
4.9
作者:
Hancks DC;Kazazian HH Jr
通讯作者:
Kazazian HH Jr
影响因子:
48
作者:
Chin, Chen-Shan;Peluso, Paul;Schatz, Michael C.
通讯作者:
Schatz, Michael C.
影响因子:
14.9
作者:
Bailey TL;Boden M;Buske FA;Frith M;Grant CE;Clementi L;Ren J;Li WW;Noble WS
通讯作者:
Noble WS
影响因子:
64.5
作者:
Elkayam E;Kuhn CD;Tocilj A;Haase AD;Greene EM;Hannon GJ;Joshua-Tor L
通讯作者:
Joshua-Tor L