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首页> 外文期刊>Molecular and Cellular Biology >Molecular cloning of five individual stage- and tissue-specific mRNA sequences from sea urchin pluteus embryos.
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Molecular cloning of five individual stage- and tissue-specific mRNA sequences from sea urchin pluteus embryos.

机译:从海胆排骨胚胎的五个个体阶段和组织特异性mRNA序列的分子克隆。

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Five developmentally regulated sea urchin mRNA sequences which increase in abundance between the blastula and pluteus stages of development were isolated by molecular cloning of cDNA. The regulated sequences all appeared in moderately abundant mRNA molecules of pluteus cells and represented 4% of the clones tested. There were no regulated sequences detected in the 40% of the clones which hybridized to the most abundant mRNA, and the screening procedures were inadequate to detect possible regulation in the 20 to 30% of the clones presumably derived from rare-class mRNA. The reaction of 32P[cDNA] from blastula and pluteus mRNA to dots of the cloned DNAs on nitrocellulose filters indicated that the mRNAs complementary to the different cloned pluteus-specific sequences were between 3- and 47-fold more prevalent at the pluteus stage than at the blastula stage. Polyadenylated RNA from different developmental stages was transferred from electrophoretic gels to nitrocellulose filters and reacted to the different cloned sequences. The regulated mRNAs were undetectable in the RNA of 3-h embryos, became evident at the hatching blastula stage, and reached a maximum in abundance by the gastrula or pluteus stage. Certain of the clones reacted to two sizes of mRNA which did not vary coordinately with development. Transfers of RNA isolated from each of the three cell layers of pluteus embryos that were reacted to the cloned sequences revealed that two of the sequences were found in the mRNA of all three layers, two were ectoderm specific, and one was endoderm specific. Four of the regulated sequences were complementary to one or two major bands and one to at least 50 bands on Southern transfers of restriction endonuclease-digested total sea urchin DNA.
机译:通过cDNA的分子克隆,分离出了五个发育受调节的海胆mRNA序列,它们在囊胚和发育期之间的丰度增加。调节的序列均出现在中等数量的睾丸细胞的mRNA分子中,占所测试克隆的4%。在与最丰富的mRNA杂交的40%的克隆中未检测到调控序列,并且筛选程序不足以检测大概20-30%的稀有类mRNA克隆中的可能调控。囊胚和脓疱mRNA中32P [cDNA]与硝酸纤维素滤膜上克隆的DNA的点的反应表明,与不同克隆的脓肿特异性序列互补的mRNA在脓疱期的流行程度是在3到47倍之间。囊胚期。将来自不同发育阶段的聚腺苷酸RNA从电泳凝胶转移到硝酸纤维素滤膜上,并与不同的克隆序列反应。调节的mRNA在3-h胚胎的RNA中不可检测,在孵化小囊阶段变得很明显,并在下腹或下腹部达到了最大丰度。某些克隆对两种大小的mRNA起反应,而这两种大小均不会随发育而变化。从与克隆序列反应的三个侧臀胚胎细胞层中分离出的RNA的转移显示,在所有三个层的mRNA中都发现了两个序列,两个是外胚层特异性的,一个是内胚层特异性的。在限制性内切酶消化的总海胆DNA的Southern转移中,四个调控序列与一个或两个主要条带和一个至至少50个条带互补。

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