Two different RNA binding activities for the AU-rich element and the poly(A) sequence of the mouse neuronal protein mHuC

被引:88
作者
Abe, R [1 ]
Sakashita, E [1 ]
Yamamoto, K [1 ]
Sakamoto, H [1 ]
机构
[1] KOBE UNIV,FAC SCI,DEPT BIOL,NADA KU,KOBE,HYOGO 657,JAPAN
基金
日本学术振兴会;
关键词
D O I
10.1093/nar/24.24.4895
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
HuC is one of the RNA binding proteins which are suggested to play important roles in neuronal differentiation and maintenance. We cloned and sequenced cDNAs encoding a mouse protein which is homologous to human HuC (hHuC). The longest cDNA encodes a 367 amino acid protein with three RNA recognition motifs (RRMs) and displays 96% identity to hHuC. Northern blot analysis showed that two different mRNAs, of 5.3 and 4.3 kb, for mouse HuC (mHuC) are expressed specifically in brain tissue. Comparison of cDNA sequences with the corresponding genomic sequence revealed that alternative 3' splice site selection generates two closely related mHuC isoforms. Iterative in vitro RNA selection and binding analyses showed that both HuC isoforms can bind with almost identical specificity to sequences similar to the AU-rich element (ARE), which is involved in the regulation of mRNA stability. Functional domain mapping using mHuC deletion mutants showed that the first RRM binds to ARE, that the second RRM has no RNA binding activity by itself, but facilitates ARE binding by the first RRM and that the third RRM has specific binding activity for the poly(A) sequence.
引用
收藏
页码:4895 / 4901
页数:7
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