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小鼠致死性黄色(Ay)突变的多效性效应可通过一个母系表达基因的缺失以及刺鼠融合RNA的同时产生来解释。

Pleiotropic effects of the mouse lethal yellow (Ay) mutation explained by deletion of a maternally expressed gene and the simultaneous production of agouti fusion RNAs.

作者信息

Duhl D M, Stevens M E, Vrieling H, Saxon P J, Miller M W, Epstein C J, Barsh G S

机构信息

Department of Pediatrics, Stanford University School of Medicine, California 94305-5428.

出版信息

Development. 1994 Jun;120(6):1695-708. doi: 10.1242/dev.120.6.1695.

DOI:10.1242/dev.120.6.1695
PMID:8050375
Abstract

Heterozygosity for the mouse lethal yellow (Ay) mutation leads to obesity, increased tumor susceptibility and increased activity of the agouti coat color gene; homozygosity for Ay results in embryonic death around the time of implantation. Although these pleiotropic effects have not been separated by recombination, previous studies have suggested that the dominant and recessive effects result from distinct genetic lesions. Here we use a combination of genomic and cDNA cloning experiments to demonstrate that the Ay mutation is caused by a 120 kb deletion which lies centromere-proximal to the agouti coat color gene. The deletion removes coding but not 5' untranslated sequences for a ubiquitously expressed gene predicted to encode a protein similar in sequence to an RNA-binding protein, which we named Merc, for maternally expressed hnRNP C-related gene, but have renamed Raly, since the gene is nearly identical to one reported recently by Michaud et al. (Gene Dev. 7, 1203-1213, 1993). The Ay deletion results in the splicing of Merc/Raly 5' untranslated sequences to agouti protein-coding sequences, which suggests that ectopic expression of the normal agouti protein by the Ay fusion RNA is responsible for the pleiotropic effects associated with heterozygosity for Ay. We find that Merc/Raly RNA is present in the unfertilized egg and is also transcribed in preimplantation embryos. Using a PCR-based assay to determine the genotype of individual embryos from an Ay/a x Ay/a intercross, we show that, in the absence of zygotic Merc/Raly expression, Ay/Ay embryos develop to the blastocyst stage, but do not hatch from the zona pellucida or form trophoblastic outgrowths. Injection of a Merc/Raly antisense oligonucleotide into non-mutant embryos blocks development prior to the blastocyst stage, and can be rescued by coinjection of a Merc/Raly transgene. These results suggest that maternal expression of Merc/Raly plays an important role in preimplantation development and that its deletion of is sufficient to explain Ay-associated embryonic lethality.

摘要

小鼠致死性黄色(Ay)突变的杂合性会导致肥胖、肿瘤易感性增加以及刺豚鼠毛色基因活性增强;Ay的纯合性则导致在着床期左右胚胎死亡。尽管这些多效性效应尚未通过重组分离,但先前的研究表明,显性和隐性效应是由不同的基因损伤引起的。在这里,我们结合基因组和cDNA克隆实验来证明,Ay突变是由一个120 kb的缺失引起的,该缺失位于刺豚鼠毛色基因的着丝粒近端。该缺失去除了一个普遍表达基因的编码序列,但未去除其5'非翻译序列,该基因预计编码一种序列与RNA结合蛋白相似的蛋白质,我们将其命名为Merc,即母源表达的hnRNP C相关基因,但后来重新命名为Raly,因为该基因与Michaud等人最近报道的一个基因几乎相同(《基因与发育》7,1203 - 1213,1993)。Ay缺失导致Merc/Raly的5'非翻译序列与刺豚鼠蛋白编码序列拼接,这表明Ay融合RNA对正常刺豚鼠蛋白的异位表达是与Ay杂合性相关的多效性效应的原因。我们发现Merc/Raly RNA存在于未受精卵中,并且在着床前胚胎中也有转录。使用基于PCR的方法来确定Ay/a×Ay/a杂交后代中单个胚胎的基因型,我们发现,在没有合子Merc/Raly表达的情况下,Ay/Ay胚胎发育到囊胚阶段,但不会从透明带孵化或形成滋养层外突。将Merc/Raly反义寡核苷酸注射到非突变胚胎中会在囊胚阶段之前阻断发育,并且可以通过共注射Merc/Raly转基因来挽救。这些结果表明,Merc/Raly的母源表达在着床前发育中起重要作用,并且其缺失足以解释与Ay相关的胚胎致死性。

相似文献

1
Pleiotropic effects of the mouse lethal yellow (Ay) mutation explained by deletion of a maternally expressed gene and the simultaneous production of agouti fusion RNAs.小鼠致死性黄色(Ay)突变的多效性效应可通过一个母系表达基因的缺失以及刺鼠融合RNA的同时产生来解释。
Development. 1994 Jun;120(6):1695-708. doi: 10.1242/dev.120.6.1695.
2
The embryonic lethality of homozygous lethal yellow mice (Ay/Ay) is associated with the disruption of a novel RNA-binding protein.纯合致死性黄色小鼠(Ay/Ay)的胚胎致死性与一种新型RNA结合蛋白的破坏有关。
Genes Dev. 1993 Jul;7(7A):1203-13. doi: 10.1101/gad.7.7a.1203.
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A molecular model for the genetic and phenotypic characteristics of the mouse lethal yellow (Ay) mutation.小鼠致死黄色(Ay)突变的遗传和表型特征的分子模型。
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Cloning of the mouse agouti gene predicts a secreted protein ubiquitously expressed in mice carrying the lethal yellow mutation.小鼠刺鼠基因的克隆表明,在携带致死性黄色突变的小鼠中普遍表达一种分泌蛋白。
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Alternative processing of the human and mouse raly genes(1).人类和小鼠raly基因的可变加工(1)
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Neomorphic agouti mutations in obese yellow mice.肥胖黄色小鼠中的新形态刺鼠突变
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Overexpression of an Agouti cDNA in the skin of transgenic mice recapitulates dominant coat color phenotypes of spontaneous mutants.在转基因小鼠的皮肤中过表达刺豚鼠cDNA可重现自发突变体的显性毛色表型。
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Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage.一种新的显性刺鼠等位基因(Aiapy)的差异表达与甲基化状态相关,并受亲本谱系的影响。
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Ectopic expression of the agouti gene in transgenic mice causes obesity, features of type II diabetes, and yellow fur.刺豚鼠基因在转基因小鼠中的异位表达会导致肥胖、II型糖尿病特征以及黄色皮毛。
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Action site of the lethal Ay gene in the mouse embryo.小鼠胚胎中致死性Ay基因的作用位点。
Jpn J Genet. 1992 Oct;67(5):357-70. doi: 10.1266/jjg.67.357.

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