Naz R K, Kumar G, Minhas B S
Department of Obstetrics and Gynecology, Albert Einstein College of Medicine, New York, New York 10461.
J Assist Reprod Genet. 1994 Apr;11(4):208-16. doi: 10.1007/BF02211810.
The present study was conducted to investigate the expression and possible role of the c-myc protooncogene in preimplantation embryos by using reverse-transcriptase/polymerase chain reaction (RT-PCR) technique and microinjection of synthetic antisense c-myc oligonucleotide probe, respectively. Total RNA was extracted from oocytes and two cell-, four cell-, early morula-, late morula-, early blastocyst-, and late blastocyst-stage embryos, and cDNA was constructed using MMLV reverse transcriptase. Sense primer (P1) and antisense primer (P2) used were based on the c-myc gene sequence bp 1609-1629 and bp 3279-3299, respectively, that span a 1.37-kb intron. PCR-amplified products of cDNA from oocyte-, two cell-, four cell-, early and late morula-, and blastocyst-stage embryos demonstrated the expected 313-bp product in Southern blot hybridization using a c-myc specific DNA probe, with an indication of lower levels in oocytes and early morulae.
Cytoplasmic injection of the antisense c-myc oligonucleotide probe (P2) and not the sense probe (P1) into pronuclear-stage zygotes caused a significant (P = 0.02 to 0.0001) inhibition of development to blastocysts in a concentration-dependent manner, with a maximal inhibition at the first cleavage of zygotes to two cell-stage embryos. There was no effect on the P2 antisense injection on pronucleus formation.
These results indicate that the c-myc protooncogene is expressed in preimplantation embryos and may have an essential role in normal embryogenesis in mice.
本研究分别采用逆转录/聚合酶链反应(RT-PCR)技术和显微注射合成的反义c-myc寡核苷酸探针,来研究c-myc原癌基因在植入前胚胎中的表达及可能作用。从卵母细胞以及二细胞、四细胞、早期桑葚胚、晚期桑葚胚、早期囊胚和晚期囊胚阶段的胚胎中提取总RNA,使用莫洛尼氏鼠白血病病毒(MMLV)逆转录酶构建cDNA。所使用的正义引物(P1)和反义引物(P2)分别基于c-myc基因序列的1609 - 1629碱基对和3279 - 3299碱基对,它们跨越一个1.37 kb的内含子。使用c-myc特异性DNA探针进行Southern印迹杂交时,来自卵母细胞、二细胞、四细胞、早期和晚期桑葚胚以及囊胚阶段胚胎的cDNA经PCR扩增后的产物显示出预期的313碱基对产物,卵母细胞和早期桑葚胚中的水平较低。
向原核期受精卵细胞质注射反义c-myc寡核苷酸探针(P2)而非正义探针(P1),以浓度依赖方式显著(P = 0.02至0.0001)抑制发育至囊胚,在受精卵首次分裂形成二细胞期胚胎时抑制作用最大。P2反义注射对原核形成没有影响。
这些结果表明,c-myc原癌基因在植入前胚胎中表达,可能在小鼠正常胚胎发生中起重要作用。