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从迪乔治关键区域直接筛选保守的cDNA:一个新的类CDC45基因的分离

Direct selection of conserved cDNAs from the DiGeorge critical region: isolation of a novel CDC45-like gene.

作者信息

McKie J M, Wadey R B, Sutherland H F, Taylor C L, Scambler P J

机构信息

Institute of Child Health, University College London Medical School, London WC1N 1EH, UK.

出版信息

Genome Res. 1998 Aug;8(8):834-41. doi: 10.1101/gr.8.8.834.

Abstract

We have used a modified direct selection technique to detect transcripts that are both evolutionary conserved and developmentally expressed. The enrichment for homologous mouse cDNAs by use of human genomic DNA as template is shown to be an efficient and rapid approach for generating transcript maps. Deletions of human 22q11 are associated with several clinical syndromes, with overlapping phenotypes, for example, velocardiofacial syndrome (VCFS) and DiGeorge syndrome (DGS). A large number of transcriptional units exist within the defined critical region, many of which have been identified previously by direct selection. However, no single obvious candidate gene for the VCFS/DGS phenotype has yet been found. Our technique has been applied to the DiGeorge critical region and has resulted in the isolation of a novel candidate gene, Cdc45l2, similar to yeast Cdc45p. [The sequence data described in this paper have been submitted to the EMBL data library under accession nos. AJ0223728 and AF0223729.]

摘要

我们采用了一种改良的直接筛选技术来检测那些在进化上保守且在发育过程中表达的转录本。利用人类基因组DNA作为模板富集同源小鼠cDNA,这被证明是一种高效且快速的生成转录图谱的方法。人类22q11缺失与几种临床综合征相关,这些综合征具有重叠的表型,例如,腭心面综合征(VCFS)和迪格奥尔格综合征(DGS)。在定义的关键区域内存在大量转录单元,其中许多先前已通过直接筛选鉴定出来。然而,尚未找到一个明显的导致VCFS/DGS表型的候选基因。我们的技术已应用于迪格奥尔格关键区域,并导致分离出一个新的候选基因Cdc45l2,它与酵母Cdc45p相似。[本文所述的序列数据已提交至EMBL数据库,登录号为AJ0223728和AF0223729。]

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本文引用的文献

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