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通过差异宏阵列筛选分离海胆胚胎中的色素细胞特异性基因。

Isolation of pigment cell specific genes in the sea urchin embryo by differential macroarray screening.

作者信息

Calestani Cristina, Rast Jonathan P, Davidson Eric H

机构信息

Division of Biology 156-29, California Institute of Technology, Pasadena, CA 91125, USA.

出版信息

Development. 2003 Oct;130(19):4587-96. doi: 10.1242/dev.00647.

Abstract

New secondary mesenchyme specific genes, expressed exclusively in pigment cells, were isolated from sea urchin embryos using a differential screening of a macroarray cDNA library. The comparison was performed between mRNA populations of embryos having an expansion of the endo-mesodermal territory and embryos blocked in secondary mesenchyme specification. To be able to isolate transcripts with a prevalence down to five copies per cell, a subtractive hybridization procedure was employed. About 400 putative positive clones were identified and sequenced from the 5' end. Gene expression analysis was carried out on a subset of 66 clones with real time quantitative PCR and 40 clones were positive. This group of clones contained sequences highly similar to: the transcription factor glial cells missing (gcm); the polyketide synthase gene cluster (pks-gc); three different members of the flavin-containing monooxygenase gene family (fmo); and a sulfotransferase gene (sult). Using whole mount in situ hybridization, it was shown that these genes are specifically expressed in pigment cells. A functional analysis of the S. purpuratus pks and of one S. purpuratus fmo was carried out using antisense technology and it was shown that their expression is necessary for the biosynthesis of the sea urchin pigment echinochrome. The results suggest that S. purpuratus pks, fmo and sult could belong to a differentiation gene battery of pigment cells.

摘要

利用对宏阵列cDNA文库的差异筛选,从海胆胚胎中分离出了仅在色素细胞中表达的新的次生间充质特异性基因。比较了内中胚层区域扩张的胚胎和次生间充质特化受阻的胚胎的mRNA群体。为了能够分离出每个细胞中低至五个拷贝的转录本,采用了消减杂交程序。从5'端鉴定并测序了约400个推定的阳性克隆。对66个克隆的一个子集进行了实时定量PCR基因表达分析,40个克隆呈阳性。这组克隆包含与以下基因高度相似的序列:转录因子神经胶质细胞缺失(gcm);聚酮合酶基因簇(pks-gc);含黄素单加氧酶基因家族的三个不同成员(fmo);以及一个磺基转移酶基因(sult)。通过全胚胎原位杂交表明,这些基因在色素细胞中特异性表达。利用反义技术对紫色海胆pks和一个紫色海胆fmo进行了功能分析,结果表明它们的表达是海胆色素海胆紫素生物合成所必需的。结果表明,紫色海胆pks、fmo和sult可能属于色素细胞的分化基因组合。

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