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果蝇端粒反转录元件TAHRE的特性:转录、转座以及基于RNA干扰的表达调控

Characterization of Drosophila telomeric retroelement TAHRE: transcription, transpositions, and RNAi-based regulation of expression.

作者信息

Shpiz Sergey, Kwon Dmitry, Uneva Anastasiya, Kim Maria, Klenov Mikhail, Rozovsky Yakov, Georgiev Pavel, Savitsky Mikhail, Kalmykova Alla

机构信息

Department of Molecular Genetics of Cell, Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia.

出版信息

Mol Biol Evol. 2007 Nov;24(11):2535-45. doi: 10.1093/molbev/msm205. Epub 2007 Sep 21.

Abstract

Telomeres in Drosophila are maintained by transpositions of specialized telomeric retroelements HeT-A and TART rather than by the telomerase activity adding short DNA repeats to chromosome ends in other eukaryotes. A novel element TAHRE was previously found in the telomeric regions of the genome of Drosophila melanogaster stock sequenced by the Genome Project. Comparative genomic analysis confirmed by Southern analysis and in situ hybridization of polytene chromosomes reveals conserved TAHRE elements in the genomes of melanogaster subgroup species. Spontaneous attachment of TAHRE retroelement to the broken end of terminally deleted chromosome allows us to consider TAHRE as the third retrotransposon family involved in telomere maintenance in Drosophila. The abundance of TAHRE transcripts in ovaries is strongly upregulated owing to mutations in the RNA interference genes spn-E, aub, piwi, and vasa locus. spn-E mutations eliminate TAHRE-specific short RNAs in the ovaries. These data suggest that TAHRE is a conservative element involved along with HeT-A and TART in telomere maintenance and a target of the RNAi-based system in the Drosophila germ line. This study reveals similar distribution of TAHRE and HeT-A transcripts, which accumulate in the oocyte, whereas TART transcripts localize in nurse cells. Taking into account a common pattern of HeT-A and TAHRE expression, one may consider TAHRE as a source of reverse transcriptase enzymatic activity for HeT-A transpositions in ovaries.

摘要

果蝇的端粒是通过特殊的端粒逆转座子HeT-A和TART的转座来维持的,而不是像其他真核生物那样通过端粒酶活性向染色体末端添加短DNA重复序列来维持。先前在基因组计划测序的黑腹果蝇品系基因组的端粒区域发现了一种新元件TAHRE。通过Southern分析和多线染色体原位杂交证实的比较基因组分析揭示了黑腹果蝇亚组物种基因组中保守的TAHRE元件。TAHRE逆转座子自发附着到末端缺失染色体的断裂末端,这使我们能够将TAHRE视为参与果蝇端粒维持的第三个逆转座子家族。由于RNA干扰基因spn-E、aub、piwi和vasa基因座的突变,卵巢中TAHRE转录本的丰度强烈上调。spn-E突变消除了卵巢中TAHRE特异性短RNA。这些数据表明,TAHRE是一种保守元件,与HeT-A和TART一起参与端粒维持,并且是果蝇生殖系中基于RNAi系统的靶标。这项研究揭示了TAHRE和HeT-A转录本的相似分布,它们在卵母细胞中积累,而TART转录本定位于滋养细胞中。考虑到HeT-A和TAHRE表达的共同模式,人们可能会将TAHRE视为卵巢中HeT-A转座的逆转录酶酶活性来源。

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