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人及小鼠植入前胚胎中翻译起始因子1A(eIF-1A)的实时逆转录-聚合酶链反应分析

Real-time reverse transcription-polymerase chain reaction analysis of translation initiation factor 1A (eIF-1A) in human and mouse preimplantation embryos.

作者信息

Lindeberg M, Hovatta O, Ahrlund-Richter L

机构信息

Clinical Research Centre, Karolinska Institute Novum, Karolinska University Hospital, 14186 Stockholm, Sweden.

出版信息

Reprod Biomed Online. 2004 Mar;8(3):338-43. doi: 10.1016/s1472-6483(10)60914-5.

DOI:10.1016/s1472-6483(10)60914-5
PMID:15038901
Abstract

Fluorescence-monitored real-time reverse transcription-polymerase chain reaction (RT-PCR) was used to study steady state concentrations of translation initiation factor eIF-1A mRNA in mouse and human preimplantation embryos. Its expression in human embryos has not been described previously. Human oocytes, and 2-cell and 4-cell embryos all showed comparable total concentrations of eIF-1A RNA, indicating a gradual decrease in the average concentration per blastomere during these developmental stages. A 4-fold increase was observed in the 8-cell embryos. This concentration remained at the morula stage, followed by a 7- to 8-fold further increase at the blastocyst stage. Mouse preimplantation embryos already showed increased concentrations of eIF-1A RNA at the 2-cell stage. Thus, transcription levels of the eIF-1A gene are associated with embryonic gene activation (EGA) in both species. The method used, real time RT-PCR, proved to be sensitive enough to detect quantitative expression in single mouse blastomeres, the observed values for steady-state concentrations of mRNA in single blastomeres correlating well with the values for whole embryos. The possibility to study gene expression quantitatively in single blastomeres may be useful in preimplantation genetic diagnosis.

摘要

采用荧光监测实时逆转录聚合酶链反应(RT-PCR)研究小鼠和人类植入前胚胎中翻译起始因子eIF-1A mRNA的稳态浓度。此前尚未描述其在人类胚胎中的表达情况。人类卵母细胞、2细胞和4细胞胚胎中eIF-1A RNA的总浓度相当,表明在这些发育阶段每个卵裂球的平均浓度逐渐降低。在8细胞胚胎中观察到浓度增加了4倍。该浓度在桑葚胚阶段保持不变,随后在囊胚阶段进一步增加7至8倍。小鼠植入前胚胎在2细胞阶段就已显示eIF-1A RNA浓度增加。因此,eIF-1A基因的转录水平与这两个物种的胚胎基因激活(EGA)相关。所采用的实时RT-PCR方法被证明足够灵敏,能够检测单个小鼠卵裂球中的定量表达,单个卵裂球中mRNA稳态浓度的观察值与整个胚胎的值相关性良好。在单个卵裂球中定量研究基因表达的可能性可能在植入前基因诊断中有用。

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