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鉴定出一种编码蛋白酪氨酸激酶且在造血细胞中表达的人类基因(HCK)。

Identification of a human gene (HCK) that encodes a protein-tyrosine kinase and is expressed in hemopoietic cells.

作者信息

Quintrell N, Lebo R, Varmus H, Bishop J M, Pettenati M J, Le Beau M M, Diaz M O, Rowley J D

出版信息

Mol Cell Biol. 1987 Jun;7(6):2267-75. doi: 10.1128/mcb.7.6.2267-2275.1987.

Abstract

We have isolated cDNAs representing a previously unrecognized human gene that apparently encodes a protein-tyrosine kinase. We have designated the gene as HCK (hemopoietic cell kinase) because its expression is prominent in the lymphoid and myeloid lineages of hemopoiesis. Expression in granulocytic and monocytic leukemia cells increases after the cells have been induced to differentiate. The 57-kilodalton protein encoded by HCK resembles the product of the proto-oncogene c-src and is therefore likely to be a peripheral membrane protein. HCK is located on human chromosome 20 at bands q11-12, a region that is affected by interstitial deletions in some acute myeloid leukemias and myeloproliferative disorders. Our findings add to the diversity of protein-tyrosine kinases that may serve specialized functions in hemopoietic cells, and they raise the possibility that damage to HCK may contribute to the pathogenesis of some human leukemias.

摘要

我们已经分离出代表一个先前未被识别的人类基因的cDNA,该基因显然编码一种蛋白酪氨酸激酶。我们将该基因命名为HCK(造血细胞激酶),因为它在造血的淋巴和髓系谱系中表达显著。粒细胞性和单核细胞性白血病细胞在被诱导分化后,其表达会增加。HCK编码的57千道尔顿蛋白类似于原癌基因c-src的产物,因此很可能是一种外周膜蛋白。HCK位于人类20号染色体q11 - 12带,该区域在一些急性髓性白血病和骨髓增殖性疾病中会受到间质缺失的影响。我们的发现增加了可能在造血细胞中发挥特殊功能的蛋白酪氨酸激酶的多样性,并且提出了HCK受损可能导致某些人类白血病发病机制的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a86/365351/21eb69d604f7/molcellb00078-0243-a.jpg

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