Increased MKK4 Abundance with Replicative Senescence Is Linked to the Joint Reduction of Multiple MicroRNAs

被引:61
作者
Marasa, Bernard S. [1 ]
Srikantan, Subramanya [1 ]
Masuda, Kiyoshi [1 ]
Abdelmohsen, Kotb [1 ]
Kuwano, Yuki [1 ]
Yang, Xiaoling [1 ]
Martindale, Jennifer L. [1 ]
Rinker-Schaeffer, Carrie W. [2 ]
Gorospe, Myriam [1 ]
机构
[1] NIA, Cellular & Mol Biol Lab, Intramural Res Program, NIH, Baltimore, MD 21224 USA
[2] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
关键词
KINASE KINASE 4; TUMOR SUPPRESSION; CELLULAR SENESCENCE; SIGNAL-TRANSDUCTION; IN-VIVO; RNA; PROTEINS; CELLS; TRANSLATION; STRESS;
D O I
10.1126/scisignal.2000442
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
MKK4 (mitogen-activated protein kinase kinase 4) is a pivotal upstream activator of c-Jun N-terminal kinase and p38. Here, we report that the abundance of MKK4 increases in senescent human diploid fibroblasts through enhanced translation. We identified four microRNAs (miR-15b, miR-24, miR-25, and miR-141) that target the MKK4 messenger RNA (mRNA); the abundance of these microRNAs decreased during replicative senescence. Individually modulating the amount of each microRNA did not modify MKK4 abundance, but their concomitant overexpression decreased and their joint reduction increased MKK4 abundance. Reporter analyses indicated that these microRNAs acted through the MKK4 5' and 3' untranslated regions. Elevated MKK4 abundance inhibited cell proliferation and increased the phosphorylation and activity of p38 and PRAK (p38-regulated/activated protein kinase). Thus, multiple microRNAs acting on a single target, the MKK4 mRNA, collectively influence MKK4 abundance during replicative senescence.
引用
收藏
页数:8
相关论文
共 27 条
[1]   Posttranscriptional gene regulation by RNA-binding proteins during oxidative stress: implications for cellular senescence [J].
Abdelmohsen, Kotb ;
Kuwano, Yuki ;
Kim, Hyeon Ho ;
Gorospe, Myriarn .
BIOLOGICAL CHEMISTRY, 2008, 389 (03) :243-255
[2]   miR-519 reduces cell proliferation by lowering RNA-binding protein HuR levels [J].
Abdelmohsen, Kotb ;
Srikantan, Subramanya ;
Kuwano, Yuki ;
Gorospe, Myriam .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (51) :20297-20302
[3]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[4]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[5]   Senescent cells, tumor suppression, and organismal aging: Good citizens, bad neighbors [J].
Campisi, J .
CELL, 2005, 120 (04) :513-522
[6]   Mammalian MAP kinase signalling cascades [J].
Chang, LF ;
Karin, M .
NATURE, 2001, 410 (6824) :37-40
[7]   Replicative senescence: a critical review [J].
Cristofalo, VJ ;
Lorenzini, A ;
Allen, RG ;
Torres, C ;
Tresini, M .
MECHANISMS OF AGEING AND DEVELOPMENT, 2004, 125 (10-11) :827-848
[8]   Mitogen-Activated Protein Kinase Kinase 4 (MKK4) [J].
Cuenda, A .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2000, 32 (06) :581-587
[9]   A BIOMARKER THAT IDENTIFIES SENESCENT HUMAN-CELLS IN CULTURE AND IN AGING SKIN IN-VIVO [J].
DIMRI, GP ;
LEE, XH ;
BASILE, G ;
ACOSTA, M ;
SCOTT, C ;
ROSKELLEY, C ;
MEDRANO, EE ;
LINSKENS, M ;
RUBELJ, I ;
PEREIRASMITH, O ;
PEACOCKE, M ;
CAMPISI, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9363-9367
[10]   Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight? [J].
Filipowicz, Witold ;
Bhattacharyya, Suvendra N. ;
Sonenberg, Nahum .
NATURE REVIEWS GENETICS, 2008, 9 (02) :102-114