The L7Ae RNA binding motif is a multifunctional domain required for the ribosome-dependent Sec incorporation activity of Sec insertion sequence binding protein 2

被引:40
作者
Caban, Kelvin [1 ]
Kinzy, Scott A. [1 ]
Copeland, Paul R. [1 ]
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Microbiol Mol Genet & Immunol, Piscataway, NJ 08854 USA
关键词
D O I
10.1128/MCB.00632-07
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 decoding of specific UGA codons as selenocysteine is specified by the See insertion sequence (SECIS) element. Additionally, See-tRNA([Ser]Sec) and the dedicated Sec-specific elongation factor eEFSec are required but not sufficient for nonsense suppression. SECIS binding protein 2 (SBP2) is also essential for Sec incorporation, but its precise role is unknown. In addition to binding the SECIS element, SBP2 binds stably and quantitatively to ribosomes. To determine the function of the SBP2-ribosome interaction, conserved amino acids throughout the SBP2 L7Ae RNA binding motif were mutated to alanine in clusters of five. Mutant proteins were analyzed for ribosome binding, SECIS element binding, and Sec incorporation activity, allowing us to identify two distinct but interdependent sites within the L7Ae motif: (i) a core L7Ae motif required for SECIS binding and ribosome binding and (ii) an auxiliary motif involved in physical and functional interactions with the ribosome. Structural modeling of SBP2 based on the 15.5-kDa protein-U4 snRNA complex strongly supports a two-site model for L7Ae domain function within SBP2. These results provide evidence that the SBP2-ribosome interaction is essential for Sec incorporation.
引用
收藏
页码:6350 / 6360
页数:11
相关论文
共 31 条
[21]   THE HNRNP F-PROTEIN - UNIQUE PRIMARY STRUCTURE, NUCLEIC ACID-BINDING PROPERTIES, AND SUBCELLULAR-LOCALIZATION [J].
MATUNIS, MJ ;
XING, J ;
DREYFUSS, G .
NUCLEIC ACIDS RESEARCH, 1994, 22 (06) :1059-1067
[22]   Efficiency of mammalian selenocysteine incorporation [J].
Mehta, A ;
Rebsch, CM ;
Kinzy, SA ;
Fletcher, JE ;
Copeland, PR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (36) :37852-37859
[23]   The redox state of SECIS binding protein 2 controls its localization and selenocysteine incorporation function [J].
Papp, Laura V. ;
Lu, Jun ;
Striebel, Frank ;
Kennedy, Derek ;
Holmgren, Arne ;
Khanna, Kum Kum .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (13) :4895-4910
[24]   Ribosomal RNA kink-turn motif -: A flexible molecular hinge [J].
Rázga, F ;
Spacková, N ;
Réblová, K ;
Koca, J ;
Leontis, NB ;
Sponer, J .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2004, 22 (02) :183-193
[25]   RNA kink-turns as molecular elbows:: Hydration, cation binding, and large-scale dynamics [J].
Razga, Filip ;
Zacharias, Martin ;
Reblova, Kamila ;
Koca, Jaroslav ;
Sponer, Jiri .
STRUCTURE, 2006, 14 (05) :825-835
[26]   The PredictProtein server [J].
Rost, B ;
Yachdav, G ;
Liu, JF .
NUCLEIC ACIDS RESEARCH, 2004, 32 :W321-W326
[27]   Discrimination between defects in elongation fidelity and termination efficiency insights into translational provides mechanistic readthrough [J].
Salas-Marco, J ;
Bedwell, DM .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 348 (04) :801-815
[28]   The crystal structure of the Methanocaldococcus jannaschii multifunctional L7Ae RNA-binding protein reveals an induced-fit interaction with the box C/D RNAs [J].
Suryadi, J ;
Tran, EJ ;
Maxwell, ES ;
Brown, BA .
BIOCHEMISTRY, 2005, 44 (28) :9657-9672
[29]   Decoding apparatus for eukaryotic selenocysteine insertion [J].
Tujebajeva, RM ;
Copeland, PR ;
Xu, XM ;
Carlson, BA ;
Harney, JW ;
Driscoll, DM ;
Hatfield, DL ;
Berry, MJ .
EMBO REPORTS, 2000, 1 (02) :158-163
[30]   Yeast as a sensor of factors affecting the accuracy of protein synthesis [J].
Valente, L ;
Kinzy, TG .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2003, 60 (10) :2115-2130