Generation and characterization of LANP/pp32 null mice

被引:38
作者
Opal, P
Garcia, JJ
McCall, AE
Xu, BS
Weeber, EJ
Sweatt, JD
Orr, HT
Zoghbi, HY
机构
[1] Baylor Coll Med, Dept Neurol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Neurosci, Houston, TX 77030 USA
[4] Baylor Coll Med, Howard Hughes Med Inst, Houston, TX 77030 USA
[5] Univ Minnesota, Inst Human Genet, Minneapolis, MN 55455 USA
[6] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[7] Univ Minnesota, Dept Biochem, Minneapolis, MN 55455 USA
关键词
D O I
10.1128/MCB.24.8.3140-3149.2004
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 leucine-rich acidic nuclear protein (LANP) belongs to a family of evolutionarily conserved proteins that are characterized by an amino-terminal domain rich in leucine residues followed by a carboxy-terminal acidic tail. LANP has been implicated in the regulation of a variety of cellular processes including RNA transport, transcription, apoptosis, vesicular trafficking, and intracellular signaling. Abundantly expressed in the developing cerebellum, this protein has also been hypothesized to play a role in cerebellar morphogenesis. LANP has been implicated in disease biology as well, both as a mediator of toxicity in spinocerebellar ataxia type I and as a tumor suppressor in cancers of the breast and prostate. To better understand the function of this multifaceted protein, we have generated mice lacking LANP. Surprisingly, these mice are viable and fertile. In addition we could not discern any derangements in any of the major organ systems, including the nervous system, which we have studied in detail. Overall our results point to a functional redundancy of LANP's function, most likely provided by its closely related family members.
引用
收藏
页码:3140 / 3149
页数:10
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