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首页> 外文期刊>Cellular & molecular biology letters. >The telomere-specific non-LTR retrotransposons SART1 and TRAS1 are suppressed by Piwi subfamily proteins in the silkworm, Bombyx mori
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The telomere-specific non-LTR retrotransposons SART1 and TRAS1 are suppressed by Piwi subfamily proteins in the silkworm, Bombyx mori

机译:端粒特异的非LTR逆转座子SART1和TRAS1被家蚕Bowibyx mori中的Piwi亚家族蛋白抑制

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摘要

The telomere structures in Bombyx mori are thought to be maintained mainly by the transposition of the specialized telomeric retroelements SART and TRAS. The silkworm genome has telomeric TTAGG repeats and telomerase, but this telomerase displays little or no activity. Here, we report that the transcription of the telomeric retroelements SART1 and TRAS1 is suppressed by the silkworm Piwi subfamily proteins BmAgo3 and Siwi. The silkworm Piwi subfamily was found to be expressed predominantly in the gonads and early embryo, as in other model organisms, but in BmN4 cultured cells, these proteins formed granules that were separate from the nuage, which is a different behaviour pattern. The expression of TRAS1 was increased in BmN4 cells when BmAgo3 or Siwi were silenced by RNAi. Our results suggest that B. mori Piwi proteins are involved in regulating the transposition of telomeric retroelements, and that the functional piRNA pathway is conserved in BmN4 cultured cells.
机译:人们认为,家蚕中的端粒结构主要通过特异端粒反义元件SART和TRAS的转位来维持。蚕基因组具有端粒TTAGG重复序列和端粒酶,但这种端粒酶几乎没有活性。在这里,我们报告说,家蚕Piwi亚家族蛋白BmAgo3和Siwi抑制了端粒重组元件SART1和TRAS1的转录。与其他模型生物一样,发现蚕Piwi亚科主要在性腺和早期胚胎中表达,但在BmN4培养的细胞中,这些蛋白质形成了与成核分开的颗粒,这是一种不同的行为模式。当RNAi使BmAgo3或Siwi沉默时,BmN4细胞中TRAS1的表达增加。我们的结果表明,桑蚕毕赤酵母蛋白参与调节端粒端粒元件的转座,并且功能性piRNA途径在BmN4培养的细胞中是保守的。

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