Anomalous dystroglycan in carcinoma cell lines

被引:85
作者
Losasso, C
Di Tommaso, F
Sgambato, A
Ardito, R
Cittadini, A
Giardina, B
Petrucci, TC
Brancaccio, A [1 ]
机构
[1] Univ Cattolica Sacro Cuore, Ist Chim & Chim Clin, CNR, Ctr Chim Recettori, I-00168 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Ist Patol Gen, Ctr Ric Oncol Giovanni XXIII, I-00168 Rome, Italy
[3] Ist Super Sanita, Dipartimento Biol Cellulare, I-00161 Rome, Italy
来源
FEBS LETTERS | 2000年 / 484卷 / 03期
关键词
dystroglycan; protein processing; carcinoma; immunodetection; reverse transcriptase polymerase chain reaction;
D O I
10.1016/S0014-5793(00)02157-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dystroglycan is a receptor responsible for crucial interactions between extracellular matrix and cytoplasmic space. We provide the first evidence that dystroglycan is truncated, In HC11 normal murine and the 184B5 non-tumorigenic mammary human cell lines, the expected beta -dystraglycan 43 kDa band was found but human breast T47D, BT549, MCF7, colon HT29, HCT116, SW620, prostate DU145 and cervical HeLa cancer cells expressed an anomalous approximate to 31 kDa beta -dystroglycan band, alpha -Dystroglycan was udetectable in most of the cell lines in which beta -dystroglycan was found as a approximate to 31 kDa species, An anomalous approximate to 31 kDa beta -dystroglycan band was also observed in N-methyl-N-nitrosurea-induced primary rat mammary tumours, Reverse transcriptase polymerase chain reaction experiments confirmed the absence of alternative splicing events and/or expression of eventual dystroglycan isoforms, Using protein extraction procedures at low- and high-ionic strength, we demonstrated that both the 43 kDa and approximate to 31 kDa beta -dystroglycan bands harbour their transmembrane segment. (C) 2000 Federation of European Biochemical Societies, Published by Elsevier Science B,V, All rights reserved.
引用
收藏
页码:194 / 198
页数:5
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