The fragile X mental retardation protein interacts with U-rich RNAs in a yeast three-hybrid system

被引:37
|
作者
Dolzhanskaya, N
Sung, YJ
Conti, J
Currie, JR
Denman, RB
机构
[1] New York State Inst Basic Res Dev Disabil, Biochem Mol Neurobiol Lab, Dept Biol Mol, Staten Isl, NY 10314 USA
[2] Columbia Univ, Dept Anat & Cell Biol, New York, NY 10032 USA
[3] New York State Inst Basic Res Dev Disabil, Staten Isl, NY 10314 USA
关键词
D O I
10.1016/S0006-291X(03)00766-6
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
We recently identified several ESTs that bind to the fragile X mental retardation protein (FMRP) in vitro. To determine whether they interacted in vivo we performed three-hybrid screens in a Saccharomyces cerevisiae histidine auxotroph. We demonstrate that two of the ESTs support growth on histidine and transduce beta-galactosidase activity when co-expressed with FMRP under selective growth conditions. In contrast, the iron response element (IRE) RNA does not. Likewise, the ESTs do not support growth or transduce beta-galactosidase activity when co-expressed with the iron response element binding protein (IRP). Each EST is relatively small and has 40% identity with a sequence in FMR1 mRNA harboring FMRP binding determinants. Interestingly, while neither the ESTs contain a G-quartet structural motif they do contain U-rich sequences that are found in mRNA with demonstrated in vitro binding and in vivo association with FMRP. This indicates that U-rich elements comprise another motif recognized by FMRP. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:434 / 441
页数:8
相关论文
共 43 条