Generation and characterization of Atoh1-Cre knock-in mouse line

IF 2.4 4区 生物学 Q2 DEVELOPMENTAL BIOLOGY genesis Pub Date : 2010-04-13 DOI:10.1002/dvg.20633
Hua Yang, Xiaoling Xie, Min Deng, Xiaowei Chen, Lin Gan
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引用次数: 109

Abstract

Atoh1 encodes a basic helix-loop-helix (bHLH) transcription factor required for the development of the inner ear sensory epithelia, the dorsal spinal cord, brainstem, cerebellum, and intestinal secretory cells. In this study, to create a genetic tool for the research on gene function in the ear sensory organs, we generated an Atoh1-Cre knock-in mouse line by replacing the entire Atoh1 coding sequences with the Cre coding sequences. Atoh1Cre/+ mice were viable, fertile, and displayed no visible defects whereas the Atoh1Cre/Cre mice died perinatally. The spatiotemporal activities of Cre recombinase were examined by crossing Atoh1-Cre mice with the R26R-lacZ conditional reporter mice. Atoh1-Cre activities were detected in the developing inner ear, the hindbrain, the spinal cord, and the intestine. In the inner ear, Atoh1-Cre activities were confined to the sensory organs in which lacZ expression is detected in nearly all of the hair cells and in many supporting cells. Thus, Atoh1-Cre mouse line serves as a useful tool for the functional study of genes in the inner ear. In addition, our results demonstrate that Atoh1 is expressed in the common progenitors destined for both hair and supporting cells. genesis 48:407–413, 2010. © 2010 Wiley-Liss, Inc.

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Atoh1-Cre敲入小鼠细胞系的建立与表征
Atoh1编码一种基本的螺旋-环-螺旋(bHLH)转录因子,这是内耳感觉上皮、脊髓背侧、脑干、小脑和肠分泌细胞发育所必需的。在本研究中,为了创建一个研究耳感觉器官基因功能的遗传工具,我们将整个Atoh1编码序列替换为Cre编码序列,生成了一个Atoh1-Cre敲入小鼠系。Atoh1Cre/+小鼠存活,可生育,无明显缺陷,而Atoh1Cre/Cre小鼠围产期死亡。通过将Atoh1-Cre小鼠与R26R-lacZ条件报告小鼠杂交,检测Cre重组酶的时空活性。在发育中的内耳、后脑、脊髓和肠道中检测到Atoh1-Cre的活性。在内耳中,Atoh1-Cre活动仅限于感觉器官,而在几乎所有毛细胞和许多支持细胞中都检测到lacZ表达。因此,Atoh1-Cre小鼠系可作为内耳基因功能研究的有用工具。此外,我们的研究结果表明,Atoh1在毛细胞和支持细胞的共同祖细胞中都有表达。创世纪48:407 - 413,2010。©2010 Wiley-Liss, Inc
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来源期刊
genesis
genesis 生物-发育生物学
CiteScore
3.60
自引率
0.00%
发文量
40
审稿时长
6-12 weeks
期刊介绍: As of January 2000, Developmental Genetics was renamed and relaunched as genesis: The Journal of Genetics and Development, with a new scope and Editorial Board. The journal focuses on work that addresses the genetics of development and the fundamental mechanisms of embryological processes in animals and plants. With increased awareness of the interplay between genetics and evolutionary change, particularly during developmental processes, we encourage submission of manuscripts from all ecological niches. The expanded numbers of genomes for which sequencing is being completed will facilitate genetic and genomic examination of developmental issues, even if the model system does not fit the “classical genetic” mold. Therefore, we encourage submission of manuscripts from all species. Other areas of particular interest include: 1) the roles of epigenetics, microRNAs and environment on developmental processes; 2) genome-wide studies; 3) novel imaging techniques for the study of gene expression and cellular function; 4) comparative genetics and genomics and 5) animal models of human genetic and developmental disorders. genesis presents reviews, full research articles, short research letters, and state-of-the-art technology reports that promote an understanding of the function of genes and the roles they play in complex developmental processes.
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