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由伪尖毛虫中替代性DNA加工产生的一类大核染色体所编码基因的表达。

Expression of the gene encoded by a family of macronuclear chromosomes generated by alternative DNA processing in Oxytricha fallax.

作者信息

Williams K R, Herrick G

机构信息

Cellular, Viral and Molecular Biology, University of Utah School of Medicine, Salt Lake City 84132.

出版信息

Nucleic Acids Res. 1991 Sep 11;19(17):4717-24. doi: 10.1093/nar/19.17.4717.

Abstract

Hypotrichous ciliated protozoa, such as Oxytricha fallax, produce tiny chromosomes during generation of the transcriptionally active macronucleus. The 81-MAC family of macronuclear chromosomes is produced by alternative DNA processing, such that the chromosomes share a common region of 1.6 kbp. Transcription of a 1.3 kb mRNA from the common region has been analyzed. Transcription starts very near the telomere (34 bp), in a 23 bp region of pure A + T DNA. Polyadenylation sites are very near the other telomere (26 bp), also in a region of nearly pure A + T DNA. Three introns are clustered in the first third of the gene. Intron removal can follow polyadenylation, and the order of removal is not fixed. All three known sequence versions of the 81-MAC chromosomes are represented in the mRNA pool, with no evidence of any further versions. The A + T sequences surrounding the transcription starts and polyadenylation sites are conserved among versions. Introns have conserved 5' and 3' ends and a putative branch-point sequence (YYRAT), but otherwise are highly diverged and are AT-rich. A single long open reading frame, interrupted by the three introns, encodes a homolog of known mitochondrial solute carriers, and contains the codon TAA, which does not encode 'stop,' but a conserved glutamine; TAG appears also to encode glutamine. The results significantly enlarge the small data set of transcription start and polyadenylation sites, of intron features, and of translation signals for hypotrichs.

摘要

寡毛纤毛虫,如类氧毛虫,在转录活跃的大核生成过程中产生微小染色体。大核染色体的81-MAC家族是通过选择性DNA加工产生的,因此这些染色体共享一个1.6 kbp的共同区域。已对来自该共同区域的1.3 kb mRNA的转录进行了分析。转录起始点非常靠近端粒(34 bp),位于一段23 bp的纯A+T DNA区域。聚腺苷酸化位点非常靠近另一端粒(26 bp),同样位于一段几乎纯A+T DNA区域。三个内含子聚集在基因的前三分之一处。内含子的去除可以在聚腺苷酸化之后进行,并且去除顺序不固定。81-MAC染色体的所有三个已知序列版本都存在于mRNA池中,没有证据表明还有其他版本。转录起始点和聚腺苷酸化位点周围的A+T序列在各版本中是保守的。内含子具有保守的5'和3'末端以及一个推定的分支点序列(YYRAT),但除此之外高度分化且富含AT。一个被三个内含子中断的单一长开放阅读框编码已知线粒体溶质载体的同源物,并包含密码子TAA,该密码子不编码“终止”,而是编码一个保守的谷氨酰胺;TAG似乎也编码谷氨酰胺。这些结果显著扩大了寡毛纤毛虫转录起始点、聚腺苷酸化位点、内含子特征和翻译信号的小数据集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2363/328714/da4c400fbb60/nar00097-0134-a.jpg

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