Schaid D J, Kunz H W, Gill T J
Genetics. 1982 Apr;100(4):615-32. doi: 10.1093/genetics/100.4.615.
The autosomal dominant mutant gene, tail anomaly lethal (Tal), of the rat is lethal when homozygous but affects tail morphology (kinks and reduced length) and body weight when heterozygous. There is no apparent sex effect on the expression of Tal. It is incompletely penetrant; has variable expressivity, which is influenced partly by its genetic background; and is not linked to the major histocompatibility complex (MHC). The heterozygous Tal gene and the homozygous grc genes, which are linked to the MHC and affect body size and fertility, interact to cause intrauterine death at a time between implantation (five to seven days post-fertilization) and 15 days of gestation. This interaction shifts the time of death from the immediate postnatal period when the homozygous grc genes act to the time during gestation when the homozygous Tal gene would cause death. This description of lethal epistatic interaction in the rat appears to be the first report of this phenomenon in mammals.
大鼠常染色体显性突变基因——尾部异常致死基因(Tal),纯合时致死,但杂合时会影响尾部形态(出现扭结和长度缩短)及体重。Tal基因的表达没有明显的性别效应。它具有不完全显性;表现出可变的表达度,部分受其遗传背景影响;并且与主要组织相容性复合体(MHC)不连锁。与MHC连锁且影响体型和生育力的杂合Tal基因和纯合grc基因相互作用,导致在着床后(受精后5至7天)到妊娠15天之间的某个时间发生宫内死亡。这种相互作用将死亡时间从纯合grc基因起作用的出生后即刻阶段,转变为纯合Tal基因会导致死亡的妊娠期间。大鼠中这种致死上位相互作用的描述似乎是哺乳动物中该现象的首次报道。