Duhl D M, Stevens M E, Vrieling H, Saxon P J, Miller M W, Epstein C J, Barsh G S
Department of Pediatrics, Stanford University School of Medicine, California 94305-5428.
Development. 1994 Jun;120(6):1695-708. doi: 10.1242/dev.120.6.1695.
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.
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。