首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >THE GENETICS OF A SMALL AUTOSOMAL REGION OF DROSOPHILA MELANOGASTER CONTAINING THE STRUCTURAL GENE FOR ALCOHOL DEHYDROGENASE. III. HYPOMORPHIC AND HYPERMORPHIC MUTATIONS AFFECTING THE EXPRESSION OF HAIRLESS
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THE GENETICS OF A SMALL AUTOSOMAL REGION OF DROSOPHILA MELANOGASTER CONTAINING THE STRUCTURAL GENE FOR ALCOHOL DEHYDROGENASE. III. HYPOMORPHIC AND HYPERMORPHIC MUTATIONS AFFECTING THE EXPRESSION OF HAIRLESS

机译:包含酒精脱氢酶结构基因的果蝇小自体区的遗传。三,影响无头发表达的亚同型和超亚型突变

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A lethal locus ( 1(2)br7;35 B6-10), near Adh on chromosome arm 2L of D. melanogaster, is identified with Plunkett's dominant suppressor of Hairless ( H ). Of eight new alleles, seven act as dominant suppressors of H, the eighth is a dominant enhancer of H. One of the suppressor alleles is both a leaky lethal and a weak suppressor of H. Confirming Nash (1970), deletions of 1(2)br7 are dominant suppressors, and duplications are dominant enhancers of H. A simple model is proposed to account for the interaction of 1(2)br7 and H, assuming that amorphic (or hypomorphic) alleles of l(2)br7 suppress H and that hypermorphic alleles enhance H.
机译:致死基因座(1(2)br7; 35 B6-10)在黑腹果蝇D. melanogaster染色体臂2L的Adh附近,被鉴定为Plunkett的无毛显性抑制因子(H)。在八个新的等位基因中,七个是H的主要抑制因子,第八个是H的主要增强因子。一个抑制性等位基因既是H的易漏致死因子,又是H的弱抑制子。Confirmation Nash(1970),缺失1(2 )br7是H的主要抑制子,重复是H的主要增强子。假设1(2)br7的无定形(或亚等位基因)等位基因抑制H和H,则提出一个简单模型来解释1(2)br7和H的相互作用。多态性等位基因增强了H.

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