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一个包含完整的兰尼碱受体(RYR1)基因的黏粒和酵母人工染色体重叠群。

A cosmid and yeast artificial chromosome contig containing the complete ryanodine receptor (RYR1) gene.

作者信息

Rouquier S, Giorgi D, Trask B, Bergmann A, Phillips M S, MacLennan D H, de Jong P

机构信息

Human Genome Center, Lawrence Livermore National Laboratory, Livermore, California 94550.

出版信息

Genomics. 1993 Aug;17(2):330-40. doi: 10.1006/geno.1993.1329.

Abstract

The ryanodine receptor (RYR1) gene is responsible for some forms of malignant hyperthermia and has been localized to 19q13.1. Central core disease is a genetic myopathy that is genetically linked to RYR1. We have identified an overlapping set of cosmid and YAC clones that spans more than 800 kb and includes the RYR1 gene (approximately 205 kb). Cosmids from this region were identified by screening three chromosome 19 cosmid libraries (11-fold coverage) with six subclones representing the entire RYR1 cDNA. Genomic sequences from positive cosmids were then used as probes to identify additional cosmids. A minimally overlapping set of 23 cosmids was assembled into two contigs on the basis of restriction fragment analysis and hybridization data. Three YAC clones were isolated by screening a human YAC library with selected cosmid inserts. Overlaps among these YACs and the cosmid contigs were determined by hybridizing YAC Alu-PCR products to cosmid DNAs. The YACs bridged the gap between the cosmid contigs and extended the contig on both sides. Fluorescence in situ hybridization experiments positioned the RYR1 contig between GPI, MAG, and D19S191 on the proximal side and D19S190, CYP2A, CYP2F, SNRPA, BCKDHA, and other markers on the distal side. The 800-kb contig of cloned reagents will facilitate the detailed characterization of the RYR1 gene and other loci that may be closely related to central core disease.

摘要

兰尼碱受体(RYR1)基因与某些类型的恶性高热有关,已定位于19q13.1。中央轴空病是一种遗传性肌病,与RYR1基因存在遗传关联。我们已鉴定出一组重叠的黏粒和酵母人工染色体(YAC)克隆,其跨度超过800 kb,包含RYR1基因(约205 kb)。通过用代表整个RYR1 cDNA的6个亚克隆筛选3个19号染色体黏粒文库(覆盖度为11倍),鉴定出该区域的黏粒。然后将阳性黏粒的基因组序列用作探针来鉴定更多黏粒。基于限制性片段分析和杂交数据,将一组最少重叠的23个黏粒组装成两个重叠群。通过用选定的黏粒插入片段筛选人YAC文库,分离出3个YAC克隆。通过将YAC Alu-PCR产物与黏粒DNA杂交,确定这些YAC与黏粒重叠群之间的重叠情况。这些YAC填补了黏粒重叠群之间的缺口,并在两侧扩展了重叠群。荧光原位杂交实验将RYR1重叠群定位在近端的GPI、MAG和D19S191之间,以及远端的D19S190、CYP2A、CYP2F、SNRPA、BCKDHA和其他标记之间。这一包含800 kb的克隆试剂重叠群将有助于对RYR1基因以及可能与中央轴空病密切相关的其他基因座进行详细表征。

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