PHF10 Is Required for Cell Proliferation in Normal and SV40-Immortalized Human Fibroblast Cells

被引:20
作者
Banga, S. S. [1 ,2 ]
Peng, L. [1 ]
Dasgupta, T. [1 ]
Palejwala, V. [2 ]
Ozer, H. L. [1 ,2 ]
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Univ Hosp Canc Ctr, Newark, NJ 07103 USA
[2] Univ Med & Dent New Jersey, Dept Microbiol & Mol Genet, Newark, NJ 07103 USA
关键词
Chromosome; 6q27; Mouse/human hybrid; RNAi; SEN6; SV40; IMMORTAL HUMAN FIBROBLASTS; EPITHELIAL OVARIAN-CANCER; DEFECTIVE SIMIAN VIRUS-40; SV40-MEDIATED IMMORTALIZATION; REPLICATIVE SENESCENCE; ALLELIC IMBALANCE; COACTIVATOR SAYP; FREQUENT LOSS; CYCLE CONTROL; PDZ DOMAIN;
D O I
10.1159/000251960
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Normal human diploid fibroblasts have limited life span in culture and undergo replicative senescence after 50-60 population doublings. On the contrary, cancer cells typically divide indefinitely and are immortal. Expression of SV40 large T and small t antigens in human fibroblasts transiently extends their life span by 20-30 population doublings and facilitates immortalization. We have identified a rearrangement in chromosome 6 shared by SV40-transformed human fibroblasts. Rearrangements involving chromosome 6 are among the most frequent in human carcinogenesis. In this paper, we extend analysis of the 6q26-q27 region, a putative site for a growth suppressor gene designated SEN6 involved in immortalization of SV40-transformed cells. Detailed molecular characterization of the rearranged chromosomes (6q*, normal appearing; and 6q(t), translocated) in the SV40-immortalized cell line HALneo by isolating each of these 2 chromosomes in mouse/HAL somatic cell hybrids is presented. Analysis of these mouse/HAL somatic cell hybrids with polymorphic and nonpolymorphic markers revealed that the 6q* has undergone a chromosomal break in the MLLT4 gene (alias AF6). This result in conjunction with previous published observations leads us to conclude that SEN6 lies between MLLT4 and TBP at chromosomal region 6q27. Examination of different genes (MLLT4, DLL1, FAM120B, PHF10) located within this interval that are expressed in HS74 normal fibroblast cells reveals that overexpression of epitope-tagged truncated PHF10 cDNAs resulted in reduced cell proliferation in multiple cell lines. Paradoxically, down-regulation of PHF10 by RNAi also resulted in loss of cell proliferation in normal fibroblast cells, indicating PHF10 function is required for cell growth. Taken together, these observations suggest that decreased cell proliferation with epitope-tagged truncated PHF10 proteins may be due to dominant negative effects or due to unregulated expression of these mutant proteins. Hence we conclude that PHF10 is not SEN6 but is required for cell growth. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:227 / 242
页数:16
相关论文
共 61 条
[1]   THE PHD FINGER - IMPLICATIONS FOR CHROMATIN-MEDIATED TRANSCRIPTIONAL REGULATION [J].
AASLAND, R ;
GIBSON, TJ ;
STEWART, AF .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (02) :56-59
[2]   Involvement of the cyclin-dependent kinase inhibitor p16 (INK4a) in replicative senescence of normal human fibroblasts [J].
Alcorta, DA ;
Xiong, Y ;
Phelps, D ;
Hannon, G ;
Beach, D ;
Barrett, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :13742-13747
[3]   COMPLEMENTATION OF V(D)J RECOMBINATION DEFECT AND X-RAY-SENSITIVITY OF SCID MOUSE CELLS BY HUMAN-CHROMOSOME-8 [J].
BANGA, SS ;
HALL, KT ;
SANDHU, AK ;
WEAVER, DT ;
ATHWAL, RS .
MUTATION RESEARCH-DNA REPAIR, 1994, 315 (03) :239-247
[4]   SEN6, a locus for SV40-mediated immortalization of human cells, maps to 6q26-27 [J].
Banga, SS ;
Kim, S ;
Hubbard, K ;
Dasgupta, T ;
Jha, KK ;
Patsalis, P ;
Hauptschein, R ;
Gamberi, B ;
DallaFavera, R ;
Kraemer, P ;
Ozer, HL .
ONCOGENE, 1997, 14 (03) :313-321
[5]   Telomere states and cell fates [J].
Blackburn, EH .
NATURE, 2000, 408 (6808) :53-56
[6]   SV40-INDUCED IMMORTALIZATION OF HUMAN-CELLS [J].
BRYAN, TM ;
REDDEL, RR .
CRITICAL REVIEWS IN ONCOGENESIS, 1994, 5 (04) :331-357
[7]   The junction-associated protein AF-6 interacts and clusters with specific EPH receptor tyrosine kinases at specialized sites of cell-cell contact in the brain [J].
Buchert, M ;
Schneider, S ;
Meskenaite, V ;
Adams, MT ;
Canaani, E ;
Baechi, T ;
Moelling, K ;
Hovens, CM .
JOURNAL OF CELL BIOLOGY, 1999, 144 (02) :361-371
[8]   AF6/s-Afadin is a dual residency protein and localizes to a novel subnuclear compartment [J].
Buchert, Michael ;
Poon, Carole ;
King, James A. J. ;
Baechi, Thomas ;
D'Abaco, Giovanna ;
Hollande, Frederic ;
Hovens, Christopher M. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 210 (01) :212-223
[9]   The transcriptional coactivator SAYP is a trithorax group signature subunit of the PBAP chromatin remodeling complex [J].
Chalkley, Gillian E. ;
Moshkin, Yuri M. ;
Langenberg, Karin ;
Bezstarosti, Karel ;
Blastyak, Andras ;
Gyurkovics, Henrik ;
Demmers, Jeroen A. A. ;
Verrijzer, C. Peter .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (09) :2920-2929
[10]   Characterization of the components of the putative mammalian sister chromatid cohesion complex [J].
Darwiche, N ;
Freeman, LA ;
Strunnikov, A .
GENE, 1999, 233 (1-2) :39-47