Human lymphoblastoid proteome analysis reveals a role for the inhibitor of acetyltransferases complex in DNA double-strand break response

• Published in: Cancer research (Chicago, Ill.) Ill.), 2006-02, Vol.66 (3), p.1473-1480
• Main Authors: DIRKSEN, Eef H. C, CLLOOS, Jacqueline, BRAAKHUIS, Boudewijn J. M, BRAKENHOFF, Ruud H, HECK, Albert J. R, SLIJPER, Monique
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Biological and medical sciences; Cell physiology; Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes; Chromosomal Proteins, Non-Histone - metabolism; Chromosomal Proteins, Non-Histone - physiology; DNA Damage; DNA Repair - physiology; Fundamental and applied biological sciences. Psychology; Histone Chaperones; Humans; Lymphocytes - metabolism; Lymphocytes - physiology; Molecular and cellular biology; Molecular Sequence Data; Neoplasm Proteins - metabolism; Neoplasm Proteins - physiology; Proteome - metabolism; Proteome - physiology; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Transcription Factors - metabolism; Transcription Factors - physiology
• ISSN: 0008-5472; 1538-7445
• DOI: 10.1158/0008-5472.CAN-05-2129

A DNA double-strand break (DSB) is highly cytotoxic; it emerges as the type of DNA damage that most severely affects the genomic integrity of the cell. It is essential that DNA DSBs are recognized and repaired efficiently, in particular, prior to mitosis, to prevent genomic instability and eventually, the development of cancer. To assess the pathways that are induced on DNA DSBs, 14 human lymphoblastoid cell lines were challenged with bleomycin for 30 and 240 minutes to establish the fast and more prolonged response, respectively. The proteomes of 14 lymphoblastoid cell lines were investigated to account for the variation among individuals. The primary DNA DSB response was expected to occur within the nucleus; therefore, the nuclear extracts were considered. Differential analysis was done using two-dimensional difference in gel electrophoresis; paired ANOVA statistics were used to recognize significant changes in time. Many proteins whose nuclear levels changed statistically significantly showed a fast response, i.e., within 30 minutes after bleomycin challenge. A significant number of these proteins could be assigned to known DNA DSB response processes, such as sensing DSBs (Ku70), DNA repair through effectors (high-mobility group protein 1), or cell cycle arrest at the G(2)-M phase checkpoint (14-3-3 zeta). Interestingly, the nuclear levels of all three proteins in the INHAT complex were reduced after 30 minutes of bleomycin challenge, suggesting that this complex may have a role in changing the chromatin structure, allowing the DNA repair enzymes to gain access to the DNA lesions.