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非洲爪蟾nrp-1基因的分离及其在注射后的非洲爪蟾胚胎中囊胚中期转变后的表达分析。

Isolation of the Xenopus nrp-1 gene and analysis of its expression following the midblastula transition in injected Xenopus embryos.

作者信息

O'Connell Marcia L, Rebbert Martha L, Dawid Igor B

机构信息

Laboratory of Molecular Genetics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

Department of Biology, Trenton State College, Trenton, NJ 08650, USA.

出版信息

Dev Growth Differ. 1996 Aug;38(4):439-448. doi: 10.1046/j.1440-169X.1996.t01-3-00012.x.

Abstract

During embryogenesis the differentiation of distinct tissues is marked by the expression of tissue-specific genes. In Xenopus, the neural-specific gene nrp-1 is activated following the midblastula transition (MBT), and is then expressed exclusively in developing neural tissue. To pursue an investigation of the transcriptional regulation of nrp-1, the genomic DNA encoding nrp-1 was isolated and its structure analyzed. Nrp-1 lacks a canonical TATA box proximal to the start site of transcription, but the 5' flanking sequence is highly GC-rich. Injection studies with nrp-1/chloramphenicol acetyltransferase and luciferase constructs demonstrate that in Xenopus embryos, 200 nt of the 5' flanking sequence of nrp-1 are sufficient to drive the expression of reporter genes soon after the MBT, albeit not in a tissue-specific manner. This expression is enhanced by the inclusion of larger regions of the nrp-1 gene.

摘要

在胚胎发生过程中,不同组织的分化以组织特异性基因的表达为标志。在非洲爪蟾中,神经特异性基因nrp-1在中囊胚转换(MBT)后被激活,然后仅在发育中的神经组织中表达。为了研究nrp-1的转录调控,分离了编码nrp-1的基因组DNA并分析了其结构。Nrp-1在转录起始位点近端缺乏典型的TATA框,但5'侧翼序列富含GC。用nrp-1/氯霉素乙酰转移酶和荧光素酶构建体进行的注射研究表明,在非洲爪蟾胚胎中,nrp-1的5'侧翼序列的200 nt足以在MBT后不久驱动报告基因的表达,尽管不是以组织特异性方式。通过包含nrp-1基因的更大区域,这种表达会增强。

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