Transcription factor JunD, deprived of menin, switches from growth suppressor to growth promoter

被引:95
作者
Agarwal, SK
Novotny, EA
Crabtree, JS
Weitzman, JB
Yaniv, M
Burns, AL
Chandrasekharappa, SC
Collins, FS
Spiegel, AM
Marx, SJ
机构
[1] NIDDK, Metab Dis Branch, NIH, Bethesda, MD 20892 USA
[2] NHGRI, Genome Technol Branch, NIH, Bethesda, MD 20892 USA
[3] Inst Pasteur, Dept Dev Biol, CNRS, Unit Gene Express & Dis,URA 1644, F-75015 Paris, France
[4] NIDCD, Mol Pathophysiol Sect, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1073/pnas.1834524100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Different components of the AP1 transcription factor complex appear to have distinct effects on cell proliferation and transformation. In contrast to other AN components, JwunD has been shown to inhibit cell proliferation. Also, in prior studies, JunD alone bound menin, product of the MEN1 tumor suppressor gene, and JunD's transcriptional activity was inhibited by menin, suggesting that JunD might achieve all or most of its unique properties through binding to menin. Analyses of JunD and menin effects on proliferation, morphology, and cyclin D1 in stable cell lines unmasked an unexpected growth promoting activity of JunD. Whereas stable overexpression of wild-type (wt) mouse JunD in JunD(-/-) immortalized fibroblasts inhibited their proliferation and reverted their transformed-like phenotype, overexpression of a missense mouse JunD mutant (mJunD(G42E)) with disabled binding to menin showed opposite or growth promoting effects. Similarly, stable overexpression of wt mouse JunD in wt immortalized fibroblasts inhibited growth. In contrast, its overexpression in Men1(-/-) immortalized fibroblasts enhanced their already transformed-like characteristics. To conclude, JunD changed from growth suppressor to growth promoter when its binding to menin was prevented by a JunD mutant unable to bind menin or by Men1-null genetic background.
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页码:10770 / 10775
页数:6
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