Barrier to autointegration factor interacts with the cone-rod homeobox and represses its Transactivation function

被引:107
作者
Wang, XJ
Xu, SQ
Rivolta, C
Li, LY
Peng, GH
Swain, PK
Sung, CH
Swaroop, A
Berson, EL
Dryja, TP
Chen, SM
机构
[1] Washington Univ, Sch Med, Dept Ophthalmol & Visual Sci, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[3] Harvard Univ, Massachusetts Eye & Ear Infirm, Sch Med, Ocular Mol Genet Inst, Boston, MA 02114 USA
[4] Harvard Univ, Massachusetts Eye & Ear Infirm, Sch Med, Berman Gund Lab Study Retinal Degenerat, Boston, MA 02114 USA
[5] Univ Michigan, Dept Ophthalmol & Visual Sci, Ann Arbor, MI 48105 USA
[6] Univ Michigan, Dept Human Genet, Ann Arbor, MI 48105 USA
[7] Cornell Univ, Weill Med Coll, Margaret M Dyson Vis Res Inst, Dept Cell Biol & Anat, New York, NY 10021 USA
关键词
D O I
10.1074/jbc.M207952200
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
Crx (cone-rod homeobox) is a homeodomain transcription factor implicated in regulating the expression of photoreceptor and pineal genes. To identify proteins that interact with Crx in the retina, we carried out a yeast two-hybrid screen of a retinal cDNA library. One of the identified clones encodes Baf (barrier to autointegration factor), which was previously shown to have a role in mitosis and retroviral integration. Additional biochemical assays provided supporting evidence for a Baf-Crx interaction. The Baf protein is detectable in all nuclear layers of the mouse retina, including the photo-receptors and the bipolar cells where Crx is expressed. Transient transfection assays with a rhodopsin-luciferase reporter in HEK293 cells demonstrate that overexpression of Baf represses Crx-mediated transactivation, suggesting that Baf acts as a negative regulator of Crx. Consistent with this role for Baf, an E80A mutation of CRX associated with cone-rod dystrophy has a higher than normal transactivation potency but a reduced interaction with Baf. Although our studies did not identify a causative Baf mutation in retinopathies, we suggest that Baf may contribute to the phenotype of a photoreceptor degenerative disease by modifying the activity of Crx. In view of the ubiquitous expression of Baf, we hypothesize that it may play a role in regulating tissue- or cell type-specific gene expression by interacting with homeodomain transcription factors.
引用
收藏
页码:43288 / 43300
页数:13
相关论文
共 71 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   The subcellular localization of OTX2 is cell-type specific and developmentally regulated in the mouse retina [J].
Baas, D ;
Bumsted, KM ;
Martinez, JA ;
Vaccarino, FM ;
Wikler, KC ;
Barnstable, CJ .
MOLECULAR BRAIN RESEARCH, 2000, 78 (1-2) :26-37
[3]   Bardet-Biedl syndrome: A molecular and phenotypic study of 18 families [J].
Beales, PL ;
Warner, AM ;
Hitman, GA ;
Thakker, R ;
Flinter, FA .
JOURNAL OF MEDICAL GENETICS, 1997, 34 (02) :92-98
[4]   A mutation in NRL is associated with autosomal dominant retinitis pigmentosa [J].
Bessant, DAR ;
Payne, AM ;
Mitton, KP ;
Wang, QL ;
Swain, PK ;
Plant, C ;
Bird, AC ;
Zack, DJ ;
Swaroop, A ;
Bhattacharya, SS .
NATURE GENETICS, 1999, 21 (04) :355-356
[5]   Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets.: Critical differences during human and mouse eye development. [J].
Bibb, LC ;
Holt, JKL ;
Tarttelin, EE ;
Hodges, MD ;
Gregory-Evans, K ;
Rutherford, A ;
Lucas, RJ ;
Sowden, JC ;
Gregory-Evans, CY .
HUMAN MOLECULAR GENETICS, 2001, 10 (15) :1571-1579
[6]   Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes [J].
Blackshaw, S ;
Fraioli, RE ;
Furukawa, T ;
Cepko, CL .
CELL, 2001, 107 (05) :579-589
[7]   OTX2 homeodomain protein binds a DNA element necessary for interphotoreceptor retinoid binding protein gene expression [J].
Bobola, N ;
Briata, P ;
Ilengo, C ;
Rosatto, N ;
Craft, C ;
Corte, G ;
Ravazzolo, R .
MECHANISMS OF DEVELOPMENT, 1999, 82 (1-2) :165-169
[8]   Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21 [J].
Bruford, EA ;
Riise, R ;
Teague, PW ;
Porter, K ;
Thomson, KL ;
Moore, AT ;
Jay, M ;
Warburg, M ;
Schinzel, A ;
Tommerup, N ;
Tornqvist, K ;
Rosenberg, T ;
Patton, M ;
Mansfield, DC ;
Wright, AF .
GENOMICS, 1997, 41 (01) :93-99
[9]   Solution structure of the cellular factor BAF responsible for protecting retroviral DNA from autointegration [J].
Cai, M ;
Huang, Y ;
Zheng, R ;
Wei, SQ ;
Ghirlando, R ;
Lee, MS ;
Craigie, R ;
Gronenborn, AM ;
Clore, GM .
NATURE STRUCTURAL BIOLOGY, 1998, 5 (10) :903-909
[10]   MOLECULAR ANALYSIS OF THE SNF4 GENE OF SACCHAROMYCES-CEREVISIAE - EVIDENCE FOR PHYSICAL ASSOCIATION OF THE SNF4 PROTEIN WITH THE SNF1 PROTEIN-KINASE [J].
CELENZA, JL ;
ENG, FJ ;
CARLSON, M .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (11) :5045-5054