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小鼠白化基因座区域的分析。III. 产前致死小鼠的死亡时间。

Analysis of the albino-locus region of the mouse. III. Time of death of prenatal lethals.

作者信息

Russell L B, Raymer G D

出版信息

Genetics. 1979 May;92(1):205-13. doi: 10.1093/genetics/92.1.205.

Abstract

The stage at which homozygotes die was determined for 28 mutations (general symbol c*) at the albino (c) locus, of which 26 had earlier been found to be probably prenatally lethal. Within each of the mutant stocks, the uterine contents of c*/c(ch) females, made pregnant either by c*/c(ch) males ("Ex" series) or by c(ch)/c(ch) males ("Co" series), were examined between 13 and 17 days postconception. Altogether, 743 females were dissected and 7197 corpora lutea (representing ovulations) counted. In selected stocks, an additional 40 and 13 females were dissected on days seven or nine, respectively.-In each of the 26 presumed prenatally lethal mutants, there was a deficiency of living fetuses in the Ex, as compared with the Co, group. Overall, this deficiency was 23.6% (expectation, 25% c*/c*). All meaningful excesses were in numbers either of moles (death shortly before, during, or just after implantation), or of early preimplantation losses. Homozygotes in none of the mutant stocks die between days nine and 19 postconception. Of 24 c-locus mutants known to be deficiencies since they lack the closely linked Mod-2, 13 clearly kill before implantation, ten around implantation, and one neonatally. The c and Mod-2 loci and the region between them are not needed for intrauterine survival.-There are indications that the distinction between early-preimplantation death and implantation death may, in a general way, be related to length of the deficiency.

摘要

已确定了白化病(c)基因座上28个突变(通用符号c*)的纯合子死亡阶段,其中26个突变先前已被发现可能在产前致死。在每个突变品系中,检查了c*/c(ch)雌性与c*/c(ch)雄性(“Ex”系列)或c(ch)/c(ch)雄性(“Co”系列)交配受孕后13至17天的子宫内容物。总共解剖了743只雌性,并统计了7197个黄体(代表排卵)。在选定的品系中,分别在第7天或第9天额外解剖了40只和13只雌性。在26个假定产前致死的突变体中,与Co组相比,Ex组中活胎数量不足。总体而言,这种不足为23.6%(预期为25% c*/c*)。所有有意义的过量情况都出现在葡萄胎数量(在着床前、着床期间或着床后不久死亡)或着床前早期损失数量上。在任何突变品系中,纯合子在受孕后第9天至19天之间都不会死亡。已知24个c基因座突变体由于缺乏紧密连锁的Mod-2而存在缺失,其中13个明显在着床前致死,10个在着床前后致死,1个在新生儿期致死。子宫内存活不需要c和Mod-2基因座以及它们之间的区域。有迹象表明,着床前早期死亡和着床死亡之间的区别可能在一般情况下与缺失的长度有关。

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Molecular mapping within the mouse albino-deletion complex.小鼠白化缺失复合体中的分子图谱分析
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