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遗传性白内障的诱导与表现

Induction and manifestation of hereditary cataracts.

作者信息

Ehling U H

出版信息

Basic Life Sci. 1985;33:345-67. doi: 10.1007/978-1-4684-4970-9_20.

Abstract

A cataract is an opacity of the lens causing a reduction of visual function. The organogenesis of the lens in various mammals is similar. Therefore, a cataract mutation in mice can be directly compared with cataracts in man. Screening for dominant cataracts in mice was combined with the scoring of specific locus mutations. This combination increases the number of scorable loci, allows the comparison of unselected and selected loci and makes possible a systematic comparison of dominant and recessive mutations. In a combined experiment, dominant cataract and specific locus mutations were scored in the same offspring of mice after treatment of spermatogonia. In radiation experiments the induced frequency of dominant cataracts in spermatogonia was after single exposure 4.5 - 5.5 X 10(-5) mutations/gamete/Gy and for specific locus mutations 1.6 - 2.8 X 10(-5) mutations/locus/Gy. In experiments with ethylnitrosourea (ENU) the induced frequency of dominant cataracts was 0.7 - 1.3 X 10(-5) (mutations/gamete)/(mg ENU/kg body weight) and for specific locus mutations 2.6 - 3.3 X 10(-6) (mutations/locus)/(mg ENU/kg body weight). The radiation-induced mutation rate can be used for the direct estimation of the genetic risk in humans. The genetically significant population dose for 19 000 offspring in Hiroshima and Nagasaki was estimated to be 1.1 X 10(6) man-rem, absorbed at high dose rate. For the 19 000 offspring one would expect less than 1 radiation-induced dominant cataract and a total of 20 - 25 dominant mutations. If the number of dominant and recessive loci are equal one would expect in addition the induction of 250 recessive mutations in this population. Chemically induced dominant cataract mutations could be used to determine the allowable level of exposure for a single compound. The genetically characterized mutations will be an ideal source for studies in the field of developmental genetics. The investigation of alpha-, beta-, and gamma-crystallins by electrophoretic methods, the activity determinations of enzymes and the systematic use of cDNA hybridization may lead to an understanding of the genesis of dominant cataracts in mice and man.

摘要

白内障是晶状体混浊导致视觉功能减退。各种哺乳动物晶状体的器官发生过程相似。因此,小鼠中的白内障突变可直接与人的白内障进行比较。小鼠显性白内障的筛选与特定基因座突变的评分相结合。这种结合增加了可评分基因座的数量,允许对未选择和已选择的基因座进行比较,并使得对显性和隐性突变进行系统比较成为可能。在一项联合实验中,在精原细胞经处理后的同一批小鼠后代中对显性白内障和特定基因座突变进行评分。在辐射实验中,单次照射后精原细胞中显性白内障的诱导频率为4.5 - 5.5×10⁻⁵突变/配子/戈瑞,特定基因座突变的诱导频率为1.6 - 2.8×10⁻⁵突变/基因座/戈瑞。在用乙基亚硝基脲(ENU)进行的实验中,显性白内障的诱导频率为0.7 - 1.3×10⁻⁵(突变/配子)/(毫克ENU/千克体重),特定基因座突变的诱导频率为2.6 - 3.3×10⁻⁶(突变/基因座)/(毫克ENU/千克体重)。辐射诱导的突变率可用于直接估计人类的遗传风险。广岛和长崎19000名后代的遗传显著人群剂量估计为1.1×10⁶人-雷姆,以高剂量率吸收。对于这19000名后代,预计辐射诱导的显性白内障少于1例,显性突变总数为20 - 25个。如果显性和隐性基因座数量相等,预计该人群中还会诱导出250个隐性突变。化学诱导的显性白内障突变可用于确定单一化合物的允许暴露水平。经过基因特征鉴定的突变将是发育遗传学领域研究的理想来源。通过电泳方法对α-、β-和γ-晶状体蛋白进行研究、酶活性测定以及系统使用cDNA杂交可能有助于了解小鼠和人类显性白内障的发生机制。

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