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来自酵母人工染色体连续群的人类21号染色体21q22.1带的长程物理图谱。

A long-range physical map of human chromosome 21q22.1 band from the YAC continuum.

作者信息

Eki T, Abe M, Furuya K, Ahmad I, Fujishima N, Kishida H, Shiratori A, Onozaki T, Yokoyama K, Le Paslier D, Cohen D, Hanaoka F, Murakami Y

机构信息

Division of Human Genome Research, Tsukuba Life Science Center, The Institute of Physical and Chemical Research (RIKEN), 3-1-1 Koyadai, Tsukuba, Ibaraki 305, Japan.

出版信息

Mamm Genome. 1996 Apr;7(4):303-11. doi: 10.1007/s003359900087.

Abstract

The human Chromosome (Chr) 21q22.1 region contains several genes for cytokines and neurotransmitters and the gene for superoxide dismutase (mutant forms of which can cause familial amyotrophic lateral sclerosis). A region of approximately 5.8 Mb encompassing D21S82 and the glycinamide ribonucleotide transformylase (GART) loci was covered by overlapping YAC clones, which were contiguously ordered by clone walking with sequence-tagged site (STSs). A total of 76 markers, including 29 YAC end-specific STSs, were unambiguously ordered in this 5.8-Mb region, and the average interval between markers was 76 kb. Restriction maps of the YAC clones with rare-cutting enzymes were simultaneously prepared, and the restriction sites were aligned to obtain a consensus restriction map of the proximal region of the 21q22.1 band. The restriction map made from 44 overlapping YACs contains 54 physically assigned STSs. By integrating the consensus map of the adjacent 1.8-Mb region, we obtained a fine physical map spanning 6.5 Mb of human Chr 21q22.1. This map contains 24 precisely positioned end-specific STSs and 12 NotI-linking markers. More than 39 potential CpG islands were identified in this region and were found to be unevenly distributed. This physical map and the YACs should be useful as a reference map and as a resource for further structural analysis of the Giemsa-negative band (R-band) of Chr 21q22.1.

摘要

人类21号染色体(Chr)21q22.1区域包含多个细胞因子和神经递质基因以及超氧化物歧化酶基因(其突变形式可导致家族性肌萎缩侧索硬化症)。一个约5.8 Mb的区域,涵盖D21S82和甘氨酰胺核糖核苷酸转甲酰基酶(GART)基因座,被重叠的酵母人工染色体(YAC)克隆覆盖,这些克隆通过与序列标签位点(STS)进行染色体步移而连续排序。在这个5.8 Mb的区域中,总共明确排序了76个标记,包括29个YAC末端特异性STS,标记之间的平均间隔为76 kb。同时制备了用稀有切割酶处理的YAC克隆的限制酶图谱,并将限制位点对齐以获得21q22.1带近端区域的共有限制酶图谱。由44个重叠YAC制成的限制酶图谱包含54个物理定位的STS。通过整合相邻1.8 Mb区域的共有图谱,我们获得了跨越人类21号染色体21q22.1区域6.5 Mb的精细物理图谱。该图谱包含24个精确定位的末端特异性STS和12个NotI连接标记。在该区域鉴定出超过39个潜在的CpG岛,并且发现它们分布不均。这个物理图谱和YAC克隆可作为参考图谱,并作为对21q22.1染色体的吉姆萨阴性带(R带)进行进一步结构分析的资源。

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