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与唐氏综合征中阿尔茨海默病和异常骨髓生成相关的21号染色体长臂11区细菌重叠群图谱。

Bacterial contig map of the 21q11 region associated with Alzheimer's disease and abnormal myelopoiesis in Down syndrome.

作者信息

Groet J, Ives J H, South A P, Baptista P R, Jones T A, Yaspo M L, Lehrach H, Potier M C, Van Broeckhoven C, Nizetić D

机构信息

Centre for Applied Molecular Biology, School of Pharmacy, University of London, London WC1N 1AX, UK.

出版信息

Genome Res. 1998 Apr;8(4):385-98. doi: 10.1101/gr.8.4.385.

Abstract

We present a high-resolution bacterial contig map of 3.4 Mb of genomic DNA in human chromosome 21q11-q21, encompassing the region of elevated disomic homozygosity in Down Syndrome-associated abnormal myelopoiesis and leukemia, as well as the markers, which has shown a strong association with Alzheimer's Disease that has never been explained. The map contains 89 overlapping PACs, BACs, or cosmids in three contigs (850, 850, and 1500 kb) with two gaps (one of 140-210 kb and the second <5 kb). To date, eight transcribed sequences derived by cDNA selection, exon trapping, and/or global EST sequencing have been positioned onto the map, and the only two genes so far mapped to this cytogenetic region, STCH and RIP140 have been precisely localized. This work converts a further 10% of chromosome 21q into a high-resolution bacterial contig map, which will be the physical basis for the long-range sequencing of this region. The map will also enable positional derivation of new transcribed sequences, as well as new polymorphic probes, that will help in elucidation of the role the genes in this region may play in abnormal myelopoiesis and leukemia associated with trisomy 21 and Alzheimer's Disease.

摘要

我们展示了人类21号染色体q11-q21区域3.4 Mb基因组DNA的高分辨率细菌重叠群图谱,该区域涵盖唐氏综合征相关异常骨髓生成和白血病中双体纯合性升高的区域,以及与阿尔茨海默病有强烈关联但从未得到解释的标记物。该图谱包含三个重叠群(850、850和1500 kb)中的89个重叠的P1人工染色体(PAC)、细菌人工染色体(BAC)或黏粒,有两个间隙(一个140 - 210 kb,另一个<5 kb)。迄今为止,通过cDNA选择、外显子捕获和/或全局表达序列标签(EST)测序获得的八个转录序列已定位到该图谱上,并且目前仅有的两个已定位到该细胞遗传学区域的基因,即STCH和RIP140,已被精确确定位置。这项工作将21号染色体q区域另外10%转化为高分辨率细菌重叠群图谱,这将是该区域进行长距离测序的物理基础。该图谱还将有助于通过定位推导新的转录序列以及新的多态性探针,这将有助于阐明该区域基因在与21三体相关的异常骨髓生成和白血病以及阿尔茨海默病中可能发挥的作用。

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Localization of 102 exons to a 2.5 Mb region involved in Down syndrome.
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