期刊文献+

衰老相关蛋白prelamin A与MT-2A的相互作用

Interaction of aging-related protein prelamin A and MT-2A
下载PDF
导出
摘要 目的分析衰老相关蛋白prelamin A是否与MT-2A相互作用,以及MT-2A与衰老的关系。方法采用酵母双杂交方法从人骨骼肌文库中筛选prelamin A的相互作用蛋白,酵母一对一回复性杂交和荧光共定位验证MT-2A与prelamin A是否相互作用。RT-PCR分析MT-2A在正常和早老细胞中的表达。结果通过酵母双杂交方法从人骨骼肌文库中筛选到prelamin A的候选相互作用蛋白MT-2A,一对一回复性验证也证明两者能在酵母细胞中相互作用。构建含绿色荧光蛋白的MT-2A融合表达载体转染HEK-293细胞,激光共聚焦显微观察发现MT-2A能与带红色荧光蛋白的prelamin A蛋白在核膜共定位。研究还发现MT-2A的表达在早老细胞中显著下调(P<0.01)。结论 MT-2A作为一个新的prelamin A结合蛋白,可能在细胞早老过程中具有重要的作用。 Objective To analyze whether prelamin A interacts with MT-2A and the relationship of MT-2A with senescence. Methods Prelamin A binding partners were searched by a yeast two-hybrid screen using a human skeletal muscle cDNA library and validated the interaction of MT-2A with prelamin A by one to one reverse hybridization and co-localization experiment. MT-2A mRNA level was analyzed by RT-PCR. Results MT-2A was identified to interact with prelamin A by yeast two-hybrid screen and one to one reverse hybridization. MT-2A and prelamin A were co-located around nuclear envelope using laser confocal microscopy when co-transfected with pDsRed-prelamin A and pEGFP-MT-2A. RT-PCR results showed that the mRNA level of MT-2A in HEK-293prelamin A cells was significantly lower than that in HEK-293 cells (P 〈 0. 01 ). Conclusions MT-2A, as a novel prelamin A binding partner, might play a role in premature senescence.
出处 《中国老年学杂志》 CAS CSCD 北大核心 2012年第14期2972-2974,共3页 Chinese Journal of Gerontology
基金 国家自然科学基金(30672205 30871440 30971620 81000143 81170327) 广东省自然科学基金(9252402301000002 S2011010002922 8452402301001450) 广东省医学科研基金项目(B2009191 A2011431) 广东省高等学校自然科学研究重点项目(06Z015) 湛江市科技局招标项目(ZZ0605) 东莞市科技计划项目(2008108101045) 广东医学院建博科技创新基金项目(STIF201102)
关键词 MT-2A prelamin A 相互作用 酵母双杂交 衰老 MT-2A Prelamin A Interaction Yeast two-hybrid Aging
  • 相关文献

参考文献14

  • 1Liu B, Zhou Z. Lamin A/C, laminopathies and premature ageing[J]. Histol Histopath, 2008 ;23 ( 6 ) : 747-63.
  • 2Eriksson M, Brown WT, Gordon LB,et al. Recurrent de novo point mu- tations in lamin A cause Hutchinson-Gilford progeria syndrome[ J ]. Na- ture, 2003 ; 423 ( 6937 ) : 293-8.
  • 3Pendas AM. Zhou Z, Cadinanos J,et al. Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-de- ficient mice[J]. Nat Genet, 2002; (31) : 94-9.
  • 4Scaffidi P, Misteli T. Lamin A-dependent nuclear defects in human ag- ing[J]. Ss.ience, 2006; 312(5776):1059-63.
  • 5Ragnauth CD, Warren DT, Liu Y,et al. Prelamin A acts to accelerate smooth muscle cell senescence and is a novel biomarker of human vascu- lar aging[J]. Circulation, 2010; 121 (20) :2200-10.
  • 6Krishnan V, Chow MZ, Wang Z,et al. lation is associated with defective DNA in Zmpste24-deficient mice [ J ]. Proc Histone H4 lysine 16 hypoacety- repair and premature senescence Natl Acad Sci USA, 2011 ; 108 ( 30 ) : 12325-30.
  • 7Hoffman CS, Winston F. A ten-minute DNA preparation from yeast effi- ciently releases autonomous plasmids for transformation of Escherichia co- li[J]. Gene, 1987; 57(2-3) :267-72.
  • 8Campisi J, Yaswen P. Aging and cancer cell biology [ J]. Aging cell, 2009 ; 8 ( 3 ) :221-5.
  • 9Varela I, Cadinanos J, Pendas AM ,et al. Accelerated ageing in mice de- ficient in Zmpste24 protease is linked to p53 signalling activation [ J ]. Nature, 2005 ;437 ( 7058 ) :564-8.
  • 10Yamasaki M, Nomura T, Sato F,et al. Metallothionein is up-regulated under hypoxia and promotes the survival of human prostate cancer cells [J]. Oncol Rep, 2007;18(5) :1145-53.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部