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肿瘤生长过程中微管蛋白酪氨酸连接酶的抑制作用。

Suppression of tubulin tyrosine ligase during tumor growth.

作者信息

Lafanechère L, Courtay-Cahen C, Kawakami T, Jacrot M, Rüdiger M, Wehland J, Job D, Margolis R L

机构信息

Laboratoire du Cytosquelette, INSERM U366, DBMS, Commisariat a l'Energie Atomique/Grenoble, Grenoble, France.

出版信息

J Cell Sci. 1998 Jan;111 ( Pt 2):171-81. doi: 10.1242/jcs.111.2.171.

Abstract

The C terminus of the tubulin alpha-subunit of most eukaryotic cells undergoes a cycle of tyrosination and detyrosination using two specific enzymes, a tubulin tyrosine ligase (TTL) and a tubulin carboxypeptidase. Although this enzyme cycle is conserved in evolution and exhibits rapid turnover, the meaning of this modification has remained elusive. We have isolated several NIH-3T3 derived clonal cell lines that lack TTL (TTL-). TTL- cells contain a unique tubulin isotype (delta2-tubulin) that can be detected with specific antibodies. When injected into nude mice, both TTL- cells and TTL- cells stably transfected with TTL cDNA form sarcomas. But in tumors formed from TTL rescued cells, TTL is systematically lost during tumor growth. A strong selection process has thus acted during tumor growth to suppress TTL activity. In accord with this result, we find suppression of TTL activity in the majority of human tumors assayed with delta2-tubulin antibody. We conclude there is a widespread loss of TTL activity during tumor growth in situ, suggesting that TTL activity may play a role in tumor cell regulation.

摘要

大多数真核细胞微管蛋白α亚基的C末端通过两种特定的酶,即微管蛋白酪氨酸连接酶(TTL)和微管蛋白羧肽酶,经历酪氨酸化和去酪氨酸化的循环。尽管这种酶循环在进化过程中是保守的,并且周转迅速,但这种修饰的意义仍然难以捉摸。我们已经分离出了几种缺乏TTL(TTL-)的源自NIH-3T3的克隆细胞系。TTL-细胞含有一种独特的微管蛋白同种型(δ2-微管蛋白),可以用特异性抗体检测到。当注射到裸鼠体内时,TTL-细胞和稳定转染了TTL cDNA的TTL-细胞都会形成肉瘤。但是在由TTL拯救细胞形成的肿瘤中,TTL在肿瘤生长过程中会系统性地丢失。因此,在肿瘤生长过程中存在一个强烈的选择过程来抑制TTL活性。与此结果一致,我们在用δ2-微管蛋白抗体检测的大多数人类肿瘤中发现了TTL活性的抑制。我们得出结论,原位肿瘤生长过程中普遍存在TTL活性丧失的情况,这表明TTL活性可能在肿瘤细胞调节中发挥作用。

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