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人类21号染色体cDNA的分离与定位:构建21号染色体表达图谱的进展

Isolation and mapping of human chromosome 21 cDNA: progress in constructing a chromosome 21 expression map.

作者信息

Cheng J F, Boyartchuk V, Zhu Y

机构信息

Human Genome Center, Lawrence Berkeley Laboratory, California 94720.

出版信息

Genomics. 1994 Sep 1;23(1):75-84. doi: 10.1006/geno.1994.1461.

Abstract

We have isolated 175 cDNA clones from a fetal brain library by direct cDNA selection using genomic DNA isolated from pools of human chromosome 21 (HC21) cosmids. DNA sequences have revealed that 16 of these cDNA clones contain overlapping sequences. Of the other 159 cDNA sequences, 10 match previously identified HC21 genes, and 9 match previously determined cDNA sequences, including the Wilms tumor related transcript (QM), the human testican cDNA, the mammalian calponin cDNA, and 6 anonymous expressed sequence tags. All isolated cDNAs were hybridized to their corresponding cosmids, which suggests that they originated from HC21. We have localized 92 cDNA clones to previously reported HC21q YACs. The remaining unmapped cDNAs contain either sequences not included in the isolated HC21q YACs or sequences that hybridize to yeast DNA. The cDNAs not included in the YACs should be useful in isolating new YACs to bridge the gaps. PCR primers were derived from 4 novel cDNA sequences that had been mapped to the YACs in the suspected Down syndrome region and used in RT-PCR analysis. All 4 primer sequences amplified RNA fragments with the expected sizes, suggesting that these sequences could be used for expression analysis. The construction of a chromosome 21 cDNA map not only is important in the refinement of physical maps, but also will identify a set of genes in the disease regions for detailed characterization.

摘要

我们通过使用从人类21号染色体(HC21)黏粒文库中分离得到的基因组DNA进行直接cDNA筛选,从一个胎儿脑文库中分离出了175个cDNA克隆。DNA序列分析表明,其中16个cDNA克隆含有重叠序列。在其他159个cDNA序列中,10个与先前鉴定的HC21基因匹配,9个与先前确定的cDNA序列匹配,包括威尔姆斯瘤相关转录本(QM)、人类睾丸蛋白聚糖cDNA、哺乳动物钙调蛋白cDNA以及6个未知的表达序列标签。所有分离得到的cDNA都与它们相应的黏粒杂交,这表明它们起源于HC21。我们已经将92个cDNA克隆定位到先前报道的HC21q YACs上。其余未定位的cDNA要么包含分离得到的HC21q YACs中未包含的序列,要么包含与酵母DNA杂交的序列。YACs中未包含的cDNA对于分离新的YACs以填补缺口应该是有用的。PCR引物来源于4个新的cDNA序列,这些序列已被定位到疑似唐氏综合征区域的YACs上,并用于RT-PCR分析。所有4个引物序列都扩增出了预期大小的RNA片段,这表明这些序列可用于表达分析。构建21号染色体cDNA图谱不仅对于完善物理图谱很重要,而且还将鉴定出疾病区域中的一组基因进行详细表征。

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