Betts D H, MacPhee D J, Kidder G M, Watson A J
Molecular Genetics Unit, University of Western Ontario, London, Canada.
Mol Reprod Dev. 1997 Feb;46(2):114-26. doi: 10.1002/(SICI)1098-2795(199702)46:2<114::AID-MRD2>3.0.CO;2-T.
The fluid movements that arise during blastocyst formation (cavitation) are, at least in part, driven by the Na/K-ATPase. In this study, the reverse transcriptase-polymerase chain reaction (RT-PCR) was used to survey bovine pre-attachment embryos for transcripts encoding known isoforms of the Na/K-ATPase alpha- and beta-subunits, including isoforms not previously detected during the first week of mammalian development. Transcripts encoding the Na-K-ATPase alpha 1, alpha 2, alpha 3 and beta 2 isoforms were detected throughout bovine preattachment development. This is the first indication that alpha 2, alpha 3 and beta 2 mRNAs are expressed during this early developmental interval. As in the mouse, beta 1-subunit transcripts were not detected until the morula stage and were also present in blastocysts. Thus, in two mammalian species an increase in abundance of beta 1 isoform transcripts in the morula stage is coincident with the onset of cavitation. Transcripts encoding the recently characterized alpha 4 isoform were not detected. The sensitivity of bovine blastocysts to ouabain (a potent inhibitor of Na/K-ATPase) was determined by assessing the ability of bovine blastocysts to recover in ouabain supplemental culture medium following cytochalasin-induced blastocyst collapse. Re-expansion of bovine blastocysts was inhibited in all ouabain concentrations down to 10(-9) M. Mouse blastocysts, in contrast, were sensitive to ouabain at or above 10(-3)M. These results have established that transcripts encoding multiple isoforms of both the alpha and beta subunits of the Na/K-ATPase are expressed throughout early bovine development and that bovine blastocysts display a greater sensitivity to ouabain than murine blastocysts. Future analysis will determine the possible individual and collective roles of these isoforms during blastocyst formation.
囊胚形成(空泡化)过程中出现的液体流动至少部分是由钠钾ATP酶驱动的。在本研究中,逆转录聚合酶链反应(RT-PCR)用于检测牛着床前胚胎中编码钠钾ATP酶α和β亚基已知异构体的转录本,包括在哺乳动物发育第一周期间以前未检测到的异构体。在整个牛着床前发育过程中都检测到了编码钠钾ATP酶α1、α2、α3和β2异构体的转录本。这是首次表明α2、α3和β2 mRNA在这一早期发育阶段表达。与小鼠一样,直到桑葚胚阶段才检测到β1亚基转录本,囊胚中也存在该转录本。因此,在两个哺乳动物物种中,桑葚胚阶段β1异构体转录本丰度的增加与空泡化的开始同时发生。未检测到编码最近鉴定的α4异构体的转录本。通过评估细胞松弛素诱导囊胚塌陷后,牛囊胚在哇巴因补充培养基中恢复的能力,确定了牛囊胚对哇巴因(钠钾ATP酶的有效抑制剂)的敏感性。在低至10^(-9) M的所有哇巴因浓度下,牛囊胚的再扩张均受到抑制。相比之下,小鼠囊胚在10^(-3) M或更高浓度的哇巴因下敏感。这些结果表明,编码钠钾ATP酶α和β亚基多种异构体的转录本在牛早期发育过程中均有表达,并且牛囊胚对哇巴因的敏感性高于小鼠囊胚。未来的分析将确定这些异构体在囊胚形成过程中可能的个体和集体作用。