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维甲酸相关孤儿受体α缺陷小鼠的蹒跚者表型

staggerer phenotype in retinoid-related orphan receptor alpha-deficient mice.

作者信息

Steinmayr M, André E, Conquet F, Rondi-Reig L, Delhaye-Bouchaud N, Auclair N, Daniel H, Crépel F, Mariani J, Sotelo C, Becker-André M

机构信息

Geneva Biomedical Research Institute, Glaxo Wellcome Research and Development S.A., 4, chemin des Aulx, 1228 Plan-les-Ouates, Switzerland.

出版信息

Proc Natl Acad Sci U S A. 1998 Mar 31;95(7):3960-5. doi: 10.1073/pnas.95.7.3960.

Abstract

Retinoid-related orphan receptor alpha (RORalpha) is a member of the nuclear receptor superfamily. To study its physiological role we generated null-mutant mice by targeted insertion of a lacZ reporter gene encoding the enzyme beta-galactosidase. In heterozygous RORalpha+/- mice we found beta-galactosidase activity, indicative of RORalpha protein expression, confined to the central nervous system, skin and testis. In the central nervous system, the RORalpha gene is expressed in cerebellar Purkinje cells, the thalamus, the suprachiasmatic nuclei, and retinal ganglion cells. In skin, RORalpha is strongly expressed in the hair follicle, the epidermis, and the sebaceous gland. Finally, the peritubular cells of the testis and the epithelial cells of the epididymis also strongly express RORalpha. Recently, it was reported that the ataxic mouse mutant staggerer (sg/sg) is caused by a deletion in the RORalpha gene. The analysis of the cerebellar and the behavioral phenotype of homozygous RORalpha-/- mice proves identity to sg/sg mice. Although the absence of RORalpha causes dramatic developmental effects in the cerebellum, it has no apparent morphological effect on thalamus, hypothalamus, and retina. Similarly, testis and skin of RORalpha-/- mice display a normal phenotype. However, the pelage hair of both sg/sg and RORalpha-/- is significantly less dense and when shaved shows reluctance to regrow.

摘要

维甲酸相关孤儿受体α(RORα)是核受体超家族的成员。为了研究其生理作用,我们通过靶向插入编码β-半乳糖苷酶的lacZ报告基因来生成基因敲除小鼠。在杂合子RORα+/-小鼠中,我们发现β-半乳糖苷酶活性(表明RORα蛋白表达)局限于中枢神经系统、皮肤和睾丸。在中枢神经系统中,RORα基因在小脑浦肯野细胞、丘脑、视交叉上核和视网膜神经节细胞中表达。在皮肤中,RORα在毛囊、表皮和皮脂腺中强烈表达。最后,睾丸的肾小管周围细胞和附睾的上皮细胞也强烈表达RORα。最近,有报道称共济失调小鼠突变体蹒跚者(sg/sg)是由RORα基因的缺失引起的。对纯合子RORα-/-小鼠的小脑和行为表型分析证明其与sg/sg小鼠相同。尽管RORα的缺失在小脑中会引起显著的发育影响,但对丘脑、下丘脑和视网膜没有明显的形态学影响。同样,RORα-/-小鼠的睾丸和皮肤表现出正常的表型。然而,sg/sg和RORα-/-的被毛密度都明显较低,剃毛后显示出再生迟缓的现象。

相似文献

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Purkinje cell fate in staggerer mutants: agenesis versus cell death.蹒跚突变体中浦肯野细胞的命运:发育不全与细胞死亡
J Neurobiol. 2000 Feb 15;42(3):323-37. doi: 10.1002/(sici)1097-4695(20000215)42:3<323::aid-neu4>3.0.co;2-2.

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