Is post-transcriptional stabilization, splicing and translation of selective mRNAs a key to the DNA damage response?

Cell Cycle

Volumn 10, Issue 1, 2011, Pages 23-27

  Reinhardt, H Christian ^a,b   Cannell, Ian G ^c   Morandell, Sandra ^c   Yaffe, Michael B ^c,d,e  

^a UNIVERSITY HOSPITAL OF COLOGNE   (Germany)

^b Laboratory for Oncogene Signaling   (Germany)

^c David H Koch Institute for Integrative Cancer Research   (United States)

^d Massachusetts Institute of Technology Cambridge   (United States)

^e MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

Cell cycle checkpoint; DNA damage response; hnRNP A0; HuR; MAPKAP kinase 2; p38MAPK; PARN; RNA binding proteins; TIAR

Indexed keywords

DOXORUBICIN; GROWTH ARREST AND DNA DAMAGE INDUCIBLE PROTEIN 45; HISTONE H2AX; MESSENGER RNA; MITOGEN ACTIVATED PROTEIN KINASE; RNA BINDING PROTEIN;

APOPTOSIS; CELL METABOLISM; DNA DAMAGE; DOWN REGULATION; GENE EXPRESSION; GENE SILENCING; IONIZING RADIATION; LUNG SMALL CELL CANCER; LYMPHOBLASTOID CELL LINE; MASS SPECTROMETRY; PHOSPHORYLATION; POSTTRANSCRIPTIONAL GENE SILENCING; PROTEIN EXPRESSION; REVIEW; RNA SPLICING; RNA TRANSLATION; ULTRAVIOLET RADIATION;

ANIMALS; DNA DAMAGE; HUMANS; PROTEIN BIOSYNTHESIS; RNA PROCESSING, POST-TRANSCRIPTIONAL; RNA SPLICING; RNA STABILITY; RNA, MESSENGER; SIGNAL TRANSDUCTION;

EID: 78650817044     PISSN: 15384101     EISSN: 15514005     Source Type: Journal    
DOI: 10.4161/cc.10.1.14351     Document Type: Review

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