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从人嗜碱性白血病细胞系(KU812)中克隆与ZAP - 70同源的缺失型syk激酶的cDNA。

Cloning of the cDNA for the deleted syk kinase homologous to ZAP-70 from human basophilic leukemia cell line (KU812).

作者信息

Yagi S, Suzuki K, Hasegawa A, Okumura K, Ra C

机构信息

Corporate Research and Development Laboratory, Tonen Corporation, Saitama, Japan.

出版信息

Biochem Biophys Res Commun. 1994 Apr 15;200(1):28-34. doi: 10.1006/bbrc.1994.1409.

Abstract

Syk kinase is one of the protein tyrosine kinases and forms a family with ZAP-70. We isolated two different sized cDNA clones of syk (Syk11 and Syk41) from a cDNA library of human KU812 (human basophilic leukemia cell line). The obtained two clones carried different messages, that Syk41 had a 69 bp-long insertion between the SH2 domain and the kinase domain compared with Syk11. Alignment of the two human syk predicted polypeptides with those of the porcine syk and ZAP-70 revealed that human syk was 5 amino acid longer than the porcine syk at the N-termini and that the insertion of the 23 amino acid found in Syk41 was present in the porcine syk and absent in ZAP-70. Reverse transcribed polymerase chain reaction targeting this region showed that both forms of the polyA RNA were expressed in Jurkat cells, human peripheral leukocytes and also KU812 cells and that the inserted form was dominant.

摘要

Syk激酶是蛋白酪氨酸激酶之一,与ZAP-70构成一个家族。我们从人KU812(人嗜碱性白血病细胞系)的cDNA文库中分离出两个不同大小的syk cDNA克隆(Syk11和Syk41)。获得的两个克隆携带不同的信息,与Syk11相比,Syk41在SH2结构域和激酶结构域之间有一个69 bp长的插入片段。将两个人syk预测的多肽与猪syk和ZAP-70的多肽进行比对,结果显示人syk在N端比猪syk长5个氨基酸,并且Syk41中发现的23个氨基酸的插入片段存在于猪syk中,而在ZAP-70中不存在。针对该区域的逆转录聚合酶链反应表明,两种形式的polyA RNA在Jurkat细胞、人外周血白细胞以及KU812细胞中均有表达,且插入形式占主导。

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