PLC gamma 1 Src homology domain induces mitogenesis in quiescent NIH 3T3 fibroblasts

被引:35
作者
Smith, MR
Liu, YL
Kim, SR
Bae, YS
Kim, CG
Kwon, KS
Rhee, SG
Kung, HF
机构
[1] NHLBI,NIH,BIOCHEM LAB,BETHESDA,MD 20892
[2] KOREA ADV INST SCI & TECHNOL,KIBB,PROT ENGN GRP,TAEJON 305333,SOUTH KOREA
基金
美国国家卫生研究院;
关键词
D O I
10.1006/bbrc.1996.0719
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
Previously, we demonstrated that microinjection of phosphoinositide-specific phospholipase C gamma l (PLC gamma l) and lipase-defective mutants of PLC gamma l induced G(o) growth arrested NIH 3T3 fibroblasts to enter S phase of the cell cycle. These experiments suggested that regions other than the catalytic domain of PLCyl may be responsible for inducing mitogenesis. To test other regions of PLC gamma l for DNA synthesis inducing activity, cDNA fragments encoding Src homology (SH) and pleckstrin homology (PH) domains were subcloned into the bacterial expression plasmid pGEX-2TK, and the GST fusion proteins were purified. The complete PLC gamma l SH domain peptide was found to induce DNA synthesis after microinjection into growth arrested fibroblasts. Peptides containing a single SH3 domain or two SH2 domains induced a partial response that was restored to full activity if they were co-injected. The PH domain peptide did not induce DNA synthesis. Thus, both SH3 and SH2 activity combine to give maximum DNA synthesis induction, demonstrating that non-catalytic structural domains of PLC gamma l have pronounced effects on mitogenic signaling pathways. (C) 1996 Academic Press, Inc.
引用
收藏
页码:186 / 193
页数:8
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