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bcr/abl融合蛋白中的bcr序列激活酪氨酸激酶以及c-abl的微丝结合功能。

Activation of tyrosinase kinase and microfilament-binding functions of c-abl by bcr sequences in bcr/abl fusion proteins.

作者信息

McWhirter J R, Wang J Y

机构信息

Department of Biology, University of California San Diego, La Jolla 92093-0116.

出版信息

Mol Cell Biol. 1991 Mar;11(3):1553-65. doi: 10.1128/mcb.11.3.1553-1565.1991.

Abstract

Chronic myelogenous leukemia and one type of acute lymphoblastic leukemia are characterized by a 9;22 chronosome translocation in which 5' sequences of the bcr gene become fused to the c-abl proto-oncogene. The resulting chimeric genes encode bcr/abl fusion proteins which have deregulated tyrosine kinase activity and appear to play an important role in induction of these leukemias. A series of bcr/abl genes were constructed in which nested deletions of the bcr gene were fused to the c-abl gene. The fusion proteins encoded by these genes were assayed for autophosphorylation in vivo and for differences in subcellular localization. Our results demonstrate that bcr sequences activate two functions of c-abl; the tyrosine kinase activity and a previously undescribed microfilament-binding function. Two regions of bcr which activate these functions to different degrees have been mapped: amino acids 1 to 63 were strongly activating and amino acids 64 to 509 were weakly activating. The tyrosine kinase and microfilament-binding functions were not interdependent, as a kinase defective bcr/abl mutant still associated with actin filaments and a bcr/abl mutant lacking actin association still had deregulated kinase activity. Modification of actin filament functions by the bcr/abl tyrosine kinase may be an important event in leukemogenesis.

摘要

慢性粒细胞白血病和一种急性淋巴细胞白血病的特征是9号和22号染色体易位,其中bcr基因的5'端序列与c-abl原癌基因融合。产生的嵌合基因编码bcr/abl融合蛋白,其酪氨酸激酶活性失调,似乎在这些白血病的发生中起重要作用。构建了一系列bcr/abl基因,其中bcr基因的嵌套缺失与c-abl基因融合。对这些基因编码的融合蛋白进行了体内自磷酸化检测以及亚细胞定位差异检测。我们的结果表明,bcr序列激活了c-abl的两种功能;酪氨酸激酶活性和一种以前未描述的微丝结合功能。已定位了bcr中两个不同程度激活这些功能的区域:氨基酸1至63具有强烈激活作用,氨基酸64至509具有弱激活作用。酪氨酸激酶和微丝结合功能并非相互依赖,因为激酶缺陷型bcr/abl突变体仍与肌动蛋白丝相关,而缺乏肌动蛋白结合的bcr/abl突变体仍具有失调的激酶活性。bcr/abl酪氨酸激酶对肌动蛋白丝功能的修饰可能是白血病发生中的一个重要事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8a4/369443/37bbb7d8eeb2/molcellb00166-0383-a.jpg

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