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斑马鱼骨骼缺陷的影像学分析。

Radiographic analysis of zebrafish skeletal defects.

作者信息

Fisher Shannon, Jagadeeswaran Pudur, Halpern Marnie E

机构信息

Department of Embryology, Carnegie Institution of Washington, Baltimore, MD 21210, USA.

出版信息

Dev Biol. 2003 Dec 1;264(1):64-76. doi: 10.1016/s0012-1606(03)00399-3.

Abstract

Systematic identification of skeletal dysplasias in model vertebrates provides insight into the pathogenesis of human skeletal disorders and can aid in the identification of orthologous human genes. We are undertaking a mutagenesis screen for skeletal dysplasias in adult zebrafish, using radiography to detect abnormalities in skeletal anatomy and bone morphology. We have isolated chihuahua, a dominant mutation causing a general defect in bone growth. Heterozygous chihuahua fish have phenotypic similarities to human osteogenesis imperfecta, a skeletal dysplasia caused by mutations in the type I collagen genes. Mapping and molecular characterization of the chihuahua mutation indicates that the defect resides in the gene encoding the collagen I(alpha1) chain. Thus, chihuahua accurately models osteogenesis imperfecta at the biologic and molecular levels, and will prove an important resource for studies on the disease pathophysiology. Radiography is a practical screening tool to detect subtle skeletal abnormalities in the adult zebrafish. The identification of chihuahua demonstrates that mutant phenotypes analogous to human skeletal dysplasias will be discovered.

摘要

在模式脊椎动物中对骨骼发育异常进行系统鉴定,有助于深入了解人类骨骼疾病的发病机制,并有助于鉴定直系同源的人类基因。我们正在对成年斑马鱼的骨骼发育异常进行诱变筛选,利用X射线摄影术检测骨骼解剖结构和骨形态的异常。我们分离出了“吉娃娃”突变体,这是一种导致骨骼生长普遍缺陷的显性突变。杂合的“吉娃娃”鱼与人类成骨不全症具有表型相似性,成骨不全症是一种由I型胶原基因突变引起的骨骼发育异常。对“吉娃娃”突变的定位和分子特征分析表明,缺陷存在于编码I型胶原(α1)链的基因中。因此,“吉娃娃”在生物学和分子水平上准确模拟了成骨不全症,并将成为研究该疾病病理生理学的重要资源。X射线摄影术是检测成年斑马鱼细微骨骼异常的实用筛选工具。“吉娃娃”的鉴定表明,将发现与人类骨骼发育异常类似的突变表型。

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