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一种新的小鼠肢体突变鉴定出一个Twist等位基因,其表型表达需要4号染色体上的相互作用基因座。

A new mouse limb mutation identifies a Twist allele that requires interacting loci on chromosome 4 for its phenotypic expression.

作者信息

Blanc Isabelle, Bach Antoine, Lallemand Yvan, Perrin-Schmitt Fabienne, Guénet Jean-Louis, Robert Benoît

机构信息

Unité Postulante de Génétique Moléculaire de la Morphogenèse, URA CNRS 2578, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France.

出版信息

Mamm Genome. 2003 Dec;14(12):797-804. doi: 10.1007/s00335-003-2284-x.

Abstract

Pluridigite ( Pdt) is a semi-dominant mutation obtained after a mutagenesis experiment with ethyl-nitroso-urea (ENU). The mutant exhibits abnormal skeletal pattern formation characterized by the formation of extra digits (polydactyly) in the preaxial (anterior) part of the hindlimbs. The phenotype shows incomplete penetrance, depending on the genetic background. In an F2 cross with C57BL/6, the phenotype could not be associated with a single locus. Strong linkage was observed with markers located on Chromosome (Chr) 12, in a 2-cM interval between D12Mit136 and D12Mit153. This region contains the Twist gene, and we show that the [Pdt] phenotype is dependent upon a new allele of Twist. We further identified that the whole Chr 4 is associated with the [Pdt] phenotype. The Pluridigite phenotype thus results from the combination of a Twist mutant allele and at least two additional loci.

摘要

多指畸形(Pdt)是通过用乙基亚硝基脲(ENU)进行诱变实验后获得的一种半显性突变。该突变体表现出异常的骨骼模式形成,其特征是后肢的轴前(前部)部分形成额外的指(多指畸形)。该表型表现出不完全外显率,这取决于遗传背景。在与C57BL / 6的F2杂交中,该表型与单个基因座无关。在位于第12号染色体(Chr)上、D12Mit136和D12Mit153之间2厘摩间隔的标记处观察到强连锁。该区域包含Twist基因,并且我们表明[Pdt]表型依赖于Twist的一个新等位基因。我们进一步确定整个第4号染色体与[Pdt]表型相关。因此,多指畸形表型是由Twist突变等位基因和至少两个其他基因座的组合导致的。

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