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解析简单脊索动物海鞘的基因组调控网络。

Unraveling genomic regulatory networks in the simple chordate, Ciona intestinalis.

作者信息

Shi Weiyang, Levine Michael, Davidson Brad

机构信息

Department of Molecular and Cell Biology, Division of Genetics and Development, Center for Integrative Genomics, University of California, Berkeley, California 94720, USA.

出版信息

Genome Res. 2005 Dec;15(12):1668-74. doi: 10.1101/gr.3768905.

Abstract

The draft genome of the primitive chordate, Ciona intestinalis, was published three years ago. Since then, significant progress has been made in utilizing Ciona's genomic and morphological simplicity to better understand conserved chordate developmental processes. Extensive annotation and sequencing of staged EST libraries make the Ciona genome one of the best annotated among those that are publicly available. The formation of the Ciona tadpole depends on simple, well-defined cellular lineages, and it is possible to trace the lineages of key chordate tissues such as the notochord and neural tube to the fertilized egg. Electroporation methods permit the targeted expression of regulatory genes and signaling molecules in defined cell lineages, as well as the rapid identification of regulatory DNAs underlying cell-specific gene expression. The recent sequencing of a second Ciona genome (C. savignyi) permits the use of simple alignment algorithms for the identification of conserved noncoding sequences, including microRNA genes and enhancers. Detailed expression profiles are now available for almost every gene that encodes a regulatory protein or cell-signaling molecule. The combination of gene-expression profiles, comparative genome analysis, and gene-disruption assays should permit the determination of high-resolution genomic regulatory networks underlying the specification of basic chordate tissues such as the heart, blood, notochord, and neural tube.

摘要

原始脊索动物海鞘的基因组草图于三年前公布。从那时起,在利用海鞘基因组和形态学的简单性以更好地理解保守的脊索动物发育过程方面取得了重大进展。对分期EST文库进行广泛注释和测序,使海鞘基因组成为公开可用基因组中注释最好的之一。海鞘蝌蚪的形成依赖于简单且明确的细胞谱系,并且可以将脊索动物关键组织(如脊索和神经管)的谱系追溯到受精卵。电穿孔方法允许在特定细胞谱系中靶向表达调控基因和信号分子,以及快速鉴定细胞特异性基因表达背后的调控DNA。最近对第二个海鞘基因组(萨氏海鞘)的测序使得可以使用简单的比对算法来鉴定保守的非编码序列,包括微小RNA基因和增强子。现在几乎每个编码调控蛋白或细胞信号分子的基因都有详细的表达谱。基因表达谱、比较基因组分析和基因敲除试验的结合应能确定心脏、血液、脊索和神经管等基本脊索动物组织特化背后的高分辨率基因组调控网络。

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