Subcellular localization and protein interaction of the human LIMK2 gene expressing alternative transcripts with tissue-specific regulation

被引:28
作者
Osada, H
Hasada, K
Inazawa, J
Uchida, K
Ueda, R
Takahashi, T
Takahashi, T
机构
[1] AICHI CANC CTR, RES INST, LAB ULTRASTRUCT RES, CHIKUSA KU, NAGOYA, AICHI 464, JAPAN
[2] AICHI CANC CTR, RES INST, LAB CHEMOTHERAPY, CHIKUSA KU, NAGOYA, AICHI 464, JAPAN
[3] AICHI CANC CTR, RES INST, IMMUNOL LAB, CHIKUSA KU, NAGOYA, AICHI 464, JAPAN
[4] KYOTO PREFECTURAL UNIV MED, DEPT HYG, KAMIGYO KU, KYOTO 602, JAPAN
关键词
D O I
10.1006/bbrc.1996.1847
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
In our efforts to explore possible roles of proteins with a LIM domain, which is a cysteine-rich Zinc-binding motif, in differentiation and oncogenesis in the lung, we have cloned a human LIMK2 gene and identified two alternative transcripts, LIMK2a and LIMK2b, which are probably due to variation in transcriptional initiation. The former encodes a protein containing two LIM domains, a PDZ domain, and a kinase domain, while the latter has only one and half LIM domains. The predominance of the two transcripts appears to be regulated in a tissue-specific manner. Alteration of the regulation is also observed in some cancer cell lines. Transfection studies have shown an association of 63-kDa and 58-kDa proteins with the LIMK2a and LIMK2b protein; the former is distributed in the cytoplasm and nucleus and the latter occurs mainly in the cytoplasm and is scarcely translocated to the nucleus. In contrast, a truncated LIMK2-Kinase has a nuclear location, not showing the protein association. (C) 1996 Academic Press, Inc.
引用
收藏
页码:582 / 589
页数:8
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