A Genome-Wide Screen Identifies 27 Genes Involved in Transposon Silencing in C. elegans
A Genome-Wide Screen Identifies 27 Genes Involved in Transposon Silencing in C. elegans
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DOI:
10.1016/s0960-9822(03)00539-6
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发表时间:
2003-08
期刊:
影响因子:
9.2
通讯作者:
N. Vastenhouw;S. Fischer;V. Robert;K. Thijssen;A. Fraser;R. Kamath;J. Ahringer;R. Plasterk
中科院分区:
文献类型:
--
作者:
N. Vastenhouw;S. Fischer;V. Robert;K. Thijssen;A. Fraser;R. Kamath;J. Ahringer;R. Plasterk
Transposon jumps are a major cause of genome instability. In theC. elegansstrain Bristol N2, transposons are active in somatic cells, but they are silenced in the germline [1], presumably to protect the germline from mutations. Interestingly, the transposon-silencing mechanism shares factors with the RNAi machinery [2]. To better understand the mechanism of transposon silencing, we performed a genome-wide RNAi screen for genes that, when silenced, cause transposition of Tc1 in theC. elegansgermline. We identified 27 such genes, among which aremut-16, a mutator that was previously found but not identified at the molecular level,ppw-2, a member of the argonaute family, and several factors that indicate a role for chromatin structure in the regulation of transposition. Some of the newly identified genes are also required for cosuppression and therefore represent the shared components of the two pathways. Since most of the newly identified genes have clear homologs in other species, and since transposons are found from protozoa to human, it seems likely that they also protect other genomes against transposon activity in the germline.