显性半鼻疽突变的杂合子小鼠的存活率取决于遗传背景。

IF 1.3 4区 医学 Q3 PEDIATRICS Congenital Anomalies Pub Date : 2023-09-19 DOI:10.1111/cga.12541
Jun-ichi Suto
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Survival rate of mice heterozygous for the dominant hemimelia mutation depends on the genetic background
A semidominant mutation, dominant hemimelia ( Dh ), causes hindlimb malformations and congenital absence of the spleen. 1,2 Currently, the molecular nature of the Dh mutation remains unknown. Dh is maintained in the inbred mouse strain DH/Sgn by mating male asplenic DH-Dh / + mice with female eusplenic DH-+ / + mice. The Dh / + genotype is identified by the presence of hindlimb malformations and the absence of the spleen. When DH-Chr Y AKR - Dh / + (DH-Dh / + mice carrying the Y chromosome from the AKR/J strain) males were backcrossed to C57BL/6J females for two generations, many N 2 - Dh / + mice of both sexes died during weaning. 3 N 2 - Dh / + males were further backcrossed to C57BL/6J females, but Dh / + males of backcross generations further than N 5 were not obtained. Thus, Dh could not be maintained in a C57BL/6J background. This study further addressed this peculiar phenomenon. Inbred mouse strains C57BL/6J, BALB/cA, and C3H/HeJ were purchased from Clea Japan Inc. (Tokyo, Japan). Experiments were approved by the Institutional Animal Care and Use Committee of the National Institute of Agrobiological Sciences (authorization nos. H28-009 and H30-001).
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Congenital Anomalies
Congenital Anomalies PEDIATRICS-
自引率
0.00%
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49
审稿时长
>12 weeks
期刊介绍: Congenital Anomalies is the official English language journal of the Japanese Teratology Society, and publishes original articles in laboratory as well as clinical research in all areas of abnormal development and related fields, from all over the world. Although contributions by members of the teratology societies affiliated with The International Federation of Teratology Societies are given priority, contributions from non-members are welcomed.
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