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附着前牛胚胎和成体牛中碱性磷酸酶同工酶的序列和表达模式。

Sequences and expression patterns of alkaline phosphatase isozymes in preattachment bovine embryos and the adult bovine.

作者信息

McDougall K, Beecroft J, Wasnidge C, King W A, Hahnel A

机构信息

Department of Biomedical Sciences, University of Guelph, Ontario, Canada.

出版信息

Mol Reprod Dev. 1998 May;50(1):7-17. doi: 10.1002/(SICI)1098-2795(199805)50:1<7::AID-MRD2>3.0.CO;2-P.

Abstract

We report the cloning and partial sequences of two novel bovine tissue-specific alkaline phosphatase (AP) isozymes (TSAP2 and TSAP3) from in vitro-produced bovine blastocysts. Using a reverse-transcribed polymerase chain reaction (RT-PCR)-based assay for mRNA expression and in vitro-produced preattachment bovine embryos, TSAP2 mRNA was detected first at the four-cell stage prior to the major burst of embryonic transcription in cattle and TSAP3 at the eight-cell stage with the major burst in transcription. Furthermore, the transcription of TSAP2 and TSAP3 displays a curious "on-off" pattern during early cleavages between 40 and 120 hr after insemination. Activity of bovine AP, measured by an azo-dye coupling technique, indicates that at least one AP isozyme is functional in oocytes and embryos throughout bovine preattachment development. However, maternal and embryonic-derived AP activity may have different cell-surface distributions. This novel expression pattern of the bovine AP isozymes could provide a useful tool for identifying and clarifying the events controlling transcription and gene expression during early embryo development.

摘要

我们报告了从体外生产的牛囊胚中克隆出的两种新型牛组织特异性碱性磷酸酶(AP)同工酶(TSAP2和TSAP3)及其部分序列。利用基于逆转录聚合酶链反应(RT-PCR)的方法检测体外生产的牛附植前胚胎中mRNA的表达,TSAP2 mRNA在牛胚胎转录主要爆发之前的四细胞阶段首次被检测到,而TSAP3在八细胞阶段随着转录的主要爆发被检测到。此外,TSAP2和TSAP3的转录在授精后40至120小时的早期卵裂过程中呈现出一种奇特的“开-关”模式。通过偶氮染料偶联技术测量的牛AP活性表明,在牛附植前发育的整个过程中,至少有一种AP同工酶在卵母细胞和胚胎中发挥功能。然而,母体和胚胎来源的AP活性可能具有不同的细胞表面分布。牛AP同工酶的这种新表达模式可能为识别和阐明早期胚胎发育过程中控制转录和基因表达的事件提供一个有用的工具。

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