Construction and analysis of cells lacking the HMGA gene family

被引:31
作者
Beitzel, B [1 ]
Bushman, F [1 ]
机构
[1] Salk Inst Biol Studies, Infect Dis Lab, La Jolla, CA 92037 USA
关键词
D O I
10.1093/nar/gkg684
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
The high mobility group A (HMGA) family of non-histone chromosomal proteins is encoded by two related genes, HMGA1 and HMGA2. HMGA proteins are architectural transcription factors that have been found to regulate the transcription of a large number of genes. They are also some of the most commonly dysregulated genes in human neoplasias, highlighting a role in growth control. HMGA1 and HMGA2 have also been found to stimulate retroviral integration in vitro. In this study, we have cloned chicken HMGA1, and used the chicken DT40 B-cell lymphoma line to generate cells lacking HMGA1, HMGA2 and both in combination. We tested these lines for effects on cellular growth, gene control and retroviral integration. Surprisingly, we found that the HMGA gene family is dispensable for growth in DT40 cells, and that there is no apparent defect in retroviral integration in the absence of HMGA1 or HMGA2. We also analyzed the activity of approximately 4000 chicken genes, but found no significant changes. We conclude that HMGA proteins are not strictly required for growth control or retroviral integration in DT40 cells and may well be redundant with other factors.
引用
收藏
页码:5025 / 5032
页数:8
相关论文
共 50 条
[1]   In vivo modulation of Hmgic reduces obesity [J].
Anand, A ;
Chada, K .
NATURE GENETICS, 2000, 24 (04) :377-380
[2]   Genomic characterization of human HMGIC, a member of the accessory transcription factor family found at translocation breakpoints in lipomas [J].
Ashar, HR ;
Cherath, L ;
Przybysz, KM ;
Chada, K .
GENOMICS, 1996, 31 (02) :207-214
[3]   Negative regulation of BRCA1 gene expression by HMGA1 proteins accounts for the reduced BRCA1 protein levels in sporadic breast carcinoma [J].
Baldassarre, G ;
Battista, S ;
Belletti, B ;
Thakur, S ;
Pentimalli, F ;
Trapasso, F ;
Fedele, M ;
Pierantoni, G ;
Croce, CM ;
Fusco, A .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (07) :2225-2238
[4]   MINI-MOUSE - PHENOTYPIC CHARACTERIZATION OF A TRANSGENIC INSERTIONAL MUTANT ALLELIC TO PYGMY [J].
BENSON, KF ;
CHADA, K .
GENETICAL RESEARCH, 1994, 64 (01) :27-33
[5]   A comprehensive collection of chicken cDNAs [J].
Boardman, PE ;
Sanz-Ezquerro, J ;
Overton, IM ;
Burt, DW ;
Bosch, E ;
Fong, WT ;
Tickle, C ;
Brown, WRA ;
Wilson, SA ;
Hubbard, SJ .
CURRENT BIOLOGY, 2002, 12 (22) :1965-1969
[6]  
Bonnefoy E, 1999, MOL CELL BIOL, V19, P2803
[7]   Human immunodeficiency virus type 1 nucleocapsid Zn2+ fingers are required for efficient reverse transcription, initial integration processes, an protection of newly synthesized viral DNA [J].
Buckman, JS ;
Bosche, WJ ;
Gorelick, RJ .
JOURNAL OF VIROLOGY, 2003, 77 (02) :1469-1480
[8]   Coupled integration of human immunodeficiency virus type 1 cDNA ends by purified integrase in vitro: Stimulation by the viral nucleocapsid protein [J].
Carteau, S ;
Gorelick, RJ ;
Bushman, FD .
JOURNAL OF VIROLOGY, 1999, 73 (08) :6670-6679
[9]   Human immunodeficiency virus type 1 nucleocapsid protein specifically stimulates Mg2+-dependent DNA integration in vitro [J].
Carteau, S ;
Batson, SC ;
Poljak, L ;
Mouscadet, JF ;
DeRocquigny, H ;
Darlix, JL ;
Roques, BP ;
Kas, E ;
Auclair, C .
JOURNAL OF VIROLOGY, 1997, 71 (08) :6225-6229
[10]   HIV-1 integrase forms stable tetramers and associates with LEDGF/p75 protein in human cells [J].
Cherepanov, P ;
Maertens, G ;
Proost, P ;
Devreese, B ;
Van Beeumen, J ;
Engelborghs, Y ;
De Clercq, E ;
Debyser, Z .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (01) :372-381