The Freud-1/CC2D1A family: Transcriptional regulators implicated in mental retardation

被引:24
|
作者
Rogaeva, Anastasia
Galaraga, Kimberly
Albert, Paul R.
机构
[1] Univ Ottawa, Ottawa Hlth Res Inst Neurosci, Ottawa, ON K1H 8M5, Canada
[2] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON, Canada
关键词
serotonin; transcription; repression; mental; retardation; cognition;
D O I
10.1002/jnr.21277
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The CC2D1A gene family consists of two homologous genes, Freud-1/CC2D1A and Freud-2/CC2D1B, that share conserved domains, including several DM14 domains that are specific to this protein family, a C-terminal helix-loop-helix domain, and a C2 calcium-dependent phospholipid binding domain. Although the function of Freud-2 is unknown, Freud-1 has been shown to function as a transcriptional repressor of the serotonin-1A receptor gene that binds to a novel DNA element (FRE, 5'-repressor element). The DNA binding and repressor activities of Freud-1 are inhibited by calcium-calmodulin-dependent protein kinase. Recently, a deletion in the CC2D1A gene has been linked to non-syndromic mental retardation. This deletion results in the truncation of the helix-loop-helix DNA binding and the C2 domains, crucial for Freud-1 repressor activity, and hence is predicted to generate an inactive or weakly dominant negative protein. The possible mechanisms by which inactivation of Freud-1 could lead to abnormal cortical development and cognitive impairment and the potential roles of Freud-1 gene targets are discussed. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:2833 / 2838
页数:6
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