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溶组织内阿米巴u6小核RNA基因的鉴定与分析。

Identification and analysis of the u6 small nuclear RNA gene from Entamoeba histolytica.

作者信息

Miranda R, Salgado L M, Sánchez-López R, Alagón A, Lizardi P M

机构信息

Department of Molecular Recognition and Structural Biology, Instituto de Biotecnología-UNAM, Cuernavaca, Mor., Mexico.

出版信息

Gene. 1996 Nov 21;180(1-2):37-42. doi: 10.1016/s0378-1119(96)00397-6.

Abstract

Among the small nuclear RNAs (snRNAs) involved in the spliceosomal processing of pre-mRNA, U6 is the most conserved. As a first evidence for the presence of the splicing machinery in the amitochondrial protozoan Entamoeba histolytica (Eh), we have cloned the u6 snRNA gene. We find that in this organism u6 is a single copy gene that is transcribed as a poly(A)- RNA molecule of approximately 105 nucleotides. We have mapped the 5' end of the U6 snRNA transcript, and identified typical elements of a putative polymerase III promoter. This is the first snRNA gene reported in Eh. Sequence analysis indicates that this gene contains all the conserved nucleotides known to be important for U6 snRNA function. These results, in conjunction with the earlier finding of genes that contain pre-mRNA introns, suggest that Eh has a functional spliceosomal complex.

摘要

在参与前体mRNA剪接体加工的小核RNA(snRNA)中,U6是最保守的。作为线粒体原生动物溶组织内阿米巴(Eh)中存在剪接机制的首个证据,我们克隆了u6 snRNA基因。我们发现,在这种生物体中,u6是一个单拷贝基因,转录为一个约105个核苷酸的聚腺苷酸化(poly(A))RNA分子。我们已绘制出U6 snRNA转录本的5'端图谱,并鉴定出一个推定的聚合酶III启动子的典型元件。这是在Eh中报道的首个snRNA基因。序列分析表明,该基因包含所有已知对U6 snRNA功能重要的保守核苷酸。这些结果,连同早期发现的含有前体mRNA内含子的基因,表明Eh具有功能性剪接体复合物。

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