Model of the Brain Tumor-Pumilio translation repressor complex

被引:93
作者
Edwards, TA
Wilkinson, BD
Wharton, RP
Aggarwal, AK [1 ]
机构
[1] Mt Sinai Sch Med, Dept Physiol & Biophys, Struct Biol Program, New York, NY 10029 USA
[2] Duke Univ, Med Ctr, Howard Hughes Med Inst, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
关键词
Brain Tumor; Pumilio; mRNA translation; NHL domain; beta-propellor; crystal structure;
D O I
10.1101/gad.1119403
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Brain Tumor (Brat) protein is recruited to the 3' untranslated region (UTR) of hunchback mRNA to regulate its translation. Recruitment is mediated by interactions between the Pumilio RNA-binding Puf repeats and the NHL domain of Brat, a conserved structural motif present in a large family of growth regulators. In this report, we describe the crystal structure of the Brat NHL domain and present a model of the Pumilio-Brat complex derived from in silico docking experiments and supported by mutational analysis of the protein-protein interface. A key feature of the model is recognition of the outer, convex surface of the Pumilio Puf domain by the top, electropositive face of the six-bladed Brat beta-propeller. In particular, an extended loop in Puf repeat 8 fits in the entrance to the central channel of the Brat beta-propeller. Together, these interactions are likely to be prototypic of the recruitment strategies of other NHL-containing proteins in development.
引用
收藏
页码:2508 / 2513
页数:6
相关论文
共 30 条
[11]   THE DROSOPHILA POSTERIOR-GROUP GENE NANOS FUNCTIONS BY REPRESSING HUNCHBACK ACTIVITY [J].
IRISH, V ;
LEHMANN, R ;
AKAM, M .
NATURE, 1989, 338 (6217) :646-648
[12]   Implications for familial hypercholesterolemia from the structure of the LDL receptor YWTD-EGF domain pair [J].
Jeon, H ;
Meng, WY ;
Takagi, J ;
Eck, MJ ;
Springer, TA ;
Blacklow, SC .
NATURE STRUCTURAL BIOLOGY, 2001, 8 (06) :499-504
[13]   IMPROVED METHODS FOR BUILDING PROTEIN MODELS IN ELECTRON-DENSITY MAPS AND THE LOCATION OF ERRORS IN THESE MODELS [J].
JONES, TA ;
ZOU, JY ;
COWAN, SW ;
KJELDGAARD, M .
ACTA CRYSTALLOGRAPHICA SECTION A, 1991, 47 :110-119
[14]   The 2.0 angstrom crystal structure of a heterotrimeric G protein [J].
Lambright, DG ;
Sondek, J ;
Bohm, A ;
Skiba, NP ;
Hamm, HE ;
Sigler, PB .
NATURE, 1996, 379 (6563) :311-319
[15]   PROCHECK - A PROGRAM TO CHECK THE STEREOCHEMICAL QUALITY OF PROTEIN STRUCTURES [J].
LASKOWSKI, RA ;
MACARTHUR, MW ;
MOSS, DS ;
THORNTON, JM .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1993, 26 :283-291
[16]   Structural basis for phosphodependent substrate selection and orientation by the SCFCdc4 ubiquitin ligase [J].
Orlicky, S ;
Tang, XJ ;
Willems, A ;
Tyers, M ;
Sicheri, F .
CELL, 2003, 112 (02) :243-256
[17]  
Palma PN, 2000, PROTEINS, V39, P372, DOI 10.1002/(SICI)1097-0134(20000601)39:4<372::AID-PROT100>3.0.CO
[18]  
2-Q
[19]   A novel repeat domain that is often associated with RING finger and B-box motifs [J].
Slack, FJ ;
Ruvkun, G .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (12) :474-475
[20]   Crystal structure of a G(A) protein beta gamma dimer at 2.1 angstrom resolution [J].
Sondek, J ;
Bohm, A ;
Lambright, DG ;
Hamm, HE ;
Sigler, PB .
NATURE, 1996, 379 (6563) :369-374