首页> 外文期刊>Nucleic Acids Research >Molecular characterization at the RNA and gene levels of U3 snoRNA from a unicellular green alga, Chlamydomonas reinhardtii.
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Molecular characterization at the RNA and gene levels of U3 snoRNA from a unicellular green alga, Chlamydomonas reinhardtii.

机译:来自单细胞绿藻莱茵衣藻的U3 snoRNA的RNA和基因水平的分子表征。

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摘要

A U3 snoRNA gene isolated from a Chlamydomonas reinhardtii (CRE:) genomic library contains putative pol III-specific transcription signals similar to those of RNA polymerase III-specific small nuclear (sn)RNA genes of higher plants. The 222 nt long CRE: U3 snoRNA was immunoprecipitated by anti-gamma-mpppN antisera, but not by anti-m(2,2,7)G antibodies, supporting the notion that it is a RNA polymerase III transcript. Tagged CRE: U3 snoRNA gene constructs were expressed in CRE: cells. Results of chemical and enzymatic structure probing of CRE: U3 snoRNA in solution and of DMS modification of CRE: U3 snoRNA under in vivo conditions revealed that the two-hairpin structure of the 5'-domain that is found in solution is no longer detected under in vivo conditions. The observed differences can be explained by the formation of several base pair interactions with the 18S and 5'-ETS parts of the pre-rRNA. A model that involves five intermolecular helices is proposed.
机译:从莱茵衣藻(CRE :)基因组文库中分离出的U3 snoRNA基因包含推定的pol III特异性转录信号,该信号类似于高等植物的RNA聚合酶III特异性小核(sn)RNA基因。 222 nt长的CRE:U3 snoRNA是通过抗γ-mpppN抗血清免疫沉淀的,但不是通过抗m(2,2,7)G抗体免疫沉淀的,这支持了它是RNA聚合酶III转录本的观念。标记的CRE:U3 snoRNA基因构建体在CRE:细胞中表达。在体内条件下对溶液中CRE:U3 snoRNA进行化学和酶结构探测以及对CRE:U3 snoRNA进行DMS修饰的结果表明,在溶液中发现的5'结构域的两发夹结构不再存在体内条件。观察到的差异可以通过与pre-rRNA的18S和5'-ETS部分形成几个碱基对相互作用来解释。提出了一个涉及五个分子间螺旋的模型。

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