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通过BAC转基因中的一种非常规肌球蛋白纠正摇椅-2小鼠的耳聋。

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

作者信息

Probst F J, Fridell R A, Raphael Y, Saunders T L, Wang A, Liang Y, Morell R J, Touchman J W, Lyons R H, Noben-Trauth K, Friedman T B, Camper S A

机构信息

Department of Human Genetics, 4701 MSRB III, University of Michigan, 1500 West Medical Center Drive, Ann Arbor, MI 48109, USA.

出版信息

Science. 1998 May 29;280(5368):1444-7. doi: 10.1126/science.280.5368.1444.

Abstract

The shaker-2 mouse mutation, the homolog of human DFNB3, causes deafness and circling behavior. A bacterial artificial chromosome (BAC) transgene from the shaker-2 critical region corrected the vestibular defects, deafness, and inner ear morphology of shaker-2 mice. An unconventional myosin gene, Myo15, was discovered by DNA sequencing of this BAC. Shaker-2 mice were found to have an amino acid substitution at a highly conserved position within the motor domain of this myosin. Auditory hair cells of shaker-2 mice have very short stereocilia and a long actin-containing protrusion extending from their basal end. This histopathology suggests that Myo15 is necessary for actin organization in the hair cells of the cochlea.

摘要

shaker-2小鼠突变体是人类DFNB3的同源物,可导致耳聋和转圈行为。来自shaker-2关键区域的细菌人工染色体(BAC)转基因纠正了shaker-2小鼠的前庭缺陷、耳聋和内耳形态。通过对该BAC进行DNA测序,发现了一个非常规肌球蛋白基因Myo15。研究发现,shaker-2小鼠在该肌球蛋白运动结构域内一个高度保守的位置存在氨基酸替代。shaker-2小鼠的听觉毛细胞具有非常短的静纤毛,并且从其基部末端延伸出一个含肌动蛋白的长突起。这种组织病理学表明,Myo15对于耳蜗毛细胞中肌动蛋白的组织是必需的。

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