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Alkbh1 and Tzfp repress a non-repeat piRNA cluster in pachytene spermatocytes

机译:Alkbh1和Tzfp抑制粗线精子细胞中的非重复piRNA簇

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Piwi proteins and Piwi-interacting small RNAs (piRNAs) have known functions in transposon silencing in the male germline of fetal and newborn mice. Both are also present in adult testes; however, their function here remains a mystery. Here, we confirm that most piRNAs in meiotic spermatocytes originate from clusters in non-repeat intergenic regions of DNA. The regulation of these piRNA clusters, including the processing of the precursor transcripts into individual piRNAs, is accomplished through mostly unknown processes. We present a possible regulatory mechanism for one such cluster, named cluster 1082B, located on chromosome 7 in the mouse genome. The 1082B precursor transcript and its 788 unique piRNAs are repressed by the Alkbh1 dioxygenase and the testis-specific transcription repressor Tzfp. We observe a remarkable >1000-fold upregulation of individual piRNAs in pachytene spermatocytes isolated from Alkbh1- and Tzfp-deficient murine testes. Repression of cluster 1082B is further supported by the identification of a 10-bp Tzfp recognition sequence contained within the precursor transcript. Downregulation of LINE1 and IAP transcripts in the Alkbh1- and Tzfp-deficient mice leads us to propose a potential role for the 1082B-encoded piRNAs in transposon control.
机译:Piwi蛋白和与Piwi相互作用的小RNA(piRNA)在胎儿和新生小鼠的雄性种系的转座子沉默中具有已知的功能。两者也都存在于成年睾丸中。但是,它们在这里的功能仍然是个谜。在这里,我们确认减数分裂的精母细胞中的大多数piRNA起源于DNA的非重复基因间区域中的簇。这些piRNA簇的调控,包括将前体转录物加工成单个piRNA的过程,是通过大多数未知的过程完成的。我们为一个这样的群集,称为群集1082B,位于小鼠基因组7号染色体上,提出了一种可能的调控机制。 1082B前体转录物及其788个独特piRNA被Alkbh1双加氧酶和睾丸特异性转录抑制物Tzfp抑制。我们观察到分离自Alkbh1-和Tzfp缺陷小鼠睾丸的粗线精子细胞中单个piRNA的显着> 1000倍上调。鉴定包含在前体转录物中的10bp Tzfp识别序列进一步支持了对簇1082B的抑制。 Alkbh1和Tzfp缺陷小鼠中LINE1和IAP转录物的下调使我们提出了1082B编码的piRNA在转座子控制中的潜在作用。

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