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将鸡热休克蛋白90 cDNA克隆到表达载体中。

Cloning of the chick hsp 90 cDNA in expression vector.

作者信息

Catelli M G, Binart N, Feramisco J R, Helfman D M

出版信息

Nucleic Acids Res. 1985 Sep 11;13(17):6035-47. doi: 10.1093/nar/13.17.6035.

Abstract

A cDNA clone for the 90kDa heat-shock protein, which we have recently identified as a component of steroid hormone receptors in their heteromeric 8S form, was isolated by direct immunological screening of a chicken smooth muscle cDNA expression library, prepared in the expression plasmids pUC8 and pUC9. Using polyclonal and monoclonal antibodies against the 90kDa protein a colony was identified that reacted with both antibodies. Plasmid 9.11 (p9.11, approximately 1100 base pair insert) was found to hybrid-select mRNA for the 90kDa heat-shock protein. Northern blot analysis revealed that RNA isolated from various chicken tissues contain a single transcript of approximately 3 Kb hybridizing to a [32P]labelled cDNA probe made from p9.11. Heat-shock treatment of chick embryonic fibroblasts resulted in increased steady-state levels of a 3 Kb transcript in both poly A+ and poly A- RNA fractions. Southern blot analysis of chicken genomic DNA indicated that the cDNA hybridizes to a single copy sequence. Sequence data show that the p9.11 cDNA displays a high degree of homology with the 5' portion of yeast heat shock protein 90 cDNA.

摘要

我们最近鉴定出一种90kDa热休克蛋白是异源8S形式类固醇激素受体的一个组成部分,通过对用表达质粒pUC8和pUC9构建的鸡平滑肌cDNA表达文库进行直接免疫筛选,分离出了该蛋白的cDNA克隆。利用针对90kDa蛋白的多克隆抗体和单克隆抗体,鉴定出一个与两种抗体都发生反应的菌落。发现质粒9.11(p9.11,约1100个碱基对插入片段)能杂交选择90kDa热休克蛋白的mRNA。Northern印迹分析显示,从鸡的各种组织中分离的RNA含有一个约3 Kb的单一转录本,它与用p9.11制备的[32P]标记cDNA探针杂交。对鸡胚成纤维细胞进行热休克处理,导致多聚A+和多聚A-RNA组分中3 Kb转录本的稳态水平增加。对鸡基因组DNA的Southern印迹分析表明,该cDNA与单拷贝序列杂交。序列数据显示,p9.11 cDNA与酵母热休克蛋白90 cDNA的5'部分具有高度同源性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a76/321936/e364e9cbbcb5/nar00311-0031-a.jpg

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