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21号染色体上唐氏综合征关键区域的转录图谱。

A transcript map of the Down syndrome critical region on chromosome 21.

作者信息

Peterson A, Patil N, Robbins C, Wang L, Cox D R, Myers R M

机构信息

Department of Physiology, University of California at San Francisco 94143-0444.

出版信息

Hum Mol Genet. 1994 Oct;3(10):1735-42. doi: 10.1093/hmg/3.10.1735.

Abstract

A catalogue of the genes encoded by chromosome 21 would provide a framework for assigning roles in the etiology of Down syndrome (DS) to individual genes. We have begun generating such a catalogue, starting with a 1.2 Mb region surrounding the marker D21S55. Our efforts utilized the yeast artificial chromosome (YAC) and cosmid-clone based high resolution physical maps that we have constructed of this region. Direct-selection of fetal brain cDNAs with YAC DNA was used to isolate transcribed sequences. The selected cDNA fragments were analyzed by limited DNA sequence analysis, Northern blot hybridization and screening of cDNA libraries. The cDNA fragments were assigned positions on the physical map by hybridization to a collection of cosmid clones. The accurate determination of map positions for individual cDNA fragments allowed us to determine sources of variability in the cDNA selection procedure. The combined analysis and mapping was used to estimate the completeness of our mapping efforts and to identify procedures that would facilitate large-scale transcript mapping. The transcribed sequence map that we have assembled will allow the importance to DS of genes in this region to be examined and will aid in the design of strategies for larger scale efforts.

摘要

21号染色体所编码基因的目录将为确定各个基因在唐氏综合征(DS)病因学中的作用提供一个框架。我们已开始构建这样一个目录,从围绕标记D21S55的1.2 Mb区域入手。我们的工作利用了我们构建的该区域基于酵母人工染色体(YAC)和黏粒克隆的高分辨率物理图谱。用YAC DNA直接筛选胎儿脑cDNA以分离转录序列。通过有限的DNA序列分析、Northern印迹杂交和cDNA文库筛选对所选的cDNA片段进行分析。通过与一组黏粒克隆杂交,将cDNA片段定位到物理图谱上。准确确定各个cDNA片段的图谱位置使我们能够确定cDNA筛选过程中的变异来源。综合分析和定位用于评估我们图谱构建工作的完整性,并确定有助于大规模转录本定位的方法。我们组装的转录序列图谱将有助于研究该区域基因对DS的重要性,并有助于设计更大规模工作的策略。

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