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ATF-2基因缺陷小鼠的软骨发育异常和神经学异常

Chondrodysplasia and neurological abnormalities in ATF-2-deficient mice.

作者信息

Reimold A M, Grusby M J, Kosaras B, Fries J W, Mori R, Maniwa S, Clauss I M, Collins T, Sidman R L, Glimcher M J, Glimcher L H

机构信息

Department of Cancer Biology, Harvard School of Public Health, Boston, Massachusetts, USA.

出版信息

Nature. 1996 Jan 18;379(6562):262-5. doi: 10.1038/379262a0.

Abstract

Activating transcription factor-2 (ATF-2) is a basic region leucine zipper protein whose DNA target sequence is the widely distributed cAMP response element (CRE). We report here that mice carrying a germline mutation in ATF-2 demonstrated unique actions of ATF-2 not duplicated by other ATF/CREB family members. Mutant mice had decreased postnatal viability and growth, with a defect in endochondral ossification at epiphyseal plates similar to human hypochondroplasia. The animals had ataxic gait, hyperactivity and decreased hearing. In the brain, there were reduced numbers of cerebellar Purkinje cells, atrophic vestibular sense organs and enlarged ventricles. Unlike CREB alpha/delta-deficient mice whose main defect is in long-term potentiation, the widespread abnormalities in ATF-2 mutant mice demonstrate its absolute requirement for skeletal and central nervous system development, and for maximal induction of select genes with CRE sites, such as E-selectin.

摘要

激活转录因子2(ATF-2)是一种碱性区域亮氨酸拉链蛋白,其DNA靶序列是广泛分布的环磷酸腺苷反应元件(CRE)。我们在此报告,携带ATF-2种系突变的小鼠表现出ATF-2的独特作用,这是其他ATF/CREB家族成员所不具备的。突变小鼠出生后的活力和生长能力下降,骨骺板软骨内骨化存在缺陷,类似于人类软骨发育不全。这些动物步态共济失调、多动且听力下降。在大脑中,小脑浦肯野细胞数量减少,前庭感觉器官萎缩,脑室扩大。与主要缺陷在于长时程增强的CREBα/δ缺陷小鼠不同,ATF-2突变小鼠广泛存在的异常表明,其对于骨骼和中枢神经系统发育以及对具有CRE位点的特定基因(如E-选择素)的最大诱导是绝对必需的。

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