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位于3q28 - q29的显性视神经萎缩(OPA1)基因关键区域的物理图谱和转录图谱。

Physical and transcript map of the dominant optic atrophy (OPA1) gene critical region at 3q28-q29.

作者信息

Behnam J T, Hamer C, Spalton D, Johnston R, Seller M J

机构信息

Division of Medical & Molecular Genetics, Guy's Hospital, London, SE1 9RT, United Kingdom.

出版信息

Genomics. 2001 Mar 1;72(2):213-6. doi: 10.1006/geno.2000.6471.

Abstract

The dominant optic atrophy gene (OPA1) has previously been mapped to chromosome 3q28-q29. We have now constructed a physical and transcriptional map across the OPA1 critical region between markers D3S3557 and D3S3346. It comprises 21 sequence-tagged sites (STSs), 4 single nucleotide polymorphisms, 29 expressed sequence tags, 2 known genes, and 12 newly generated STSs anchored onto 21 yeast artificial chromosome, 22 bacterial artificial chromosome, 48 P1 phage artificial chromosome, and 42 cosmid overlapping clones spanning 2.5 Mb. The map has allowed us to order many of the markers hitherto only roughly defined and to exclude 23 of the putative candidate genes assigned to the region. We found the OPA1 critical interval to be 450-550 kb. It contains 2 known genes, RPL35a and SDHA, which thus constitute candidate genes.

摘要

显性遗传性视神经萎缩基因(OPA1)先前已被定位于染色体3q28 - q29。我们现已构建了跨越标记D3S3557和D3S3346之间OPA1关键区域的物理图谱和转录图谱。它包含21个序列标签位点(STS)、4个单核苷酸多态性、29个表达序列标签、2个已知基因,以及12个新生成的STS,这些STS锚定在21个酵母人工染色体、22个细菌人工染色体、48个P1噬菌体人工染色体和42个黏粒重叠克隆上,跨越2.5 Mb。该图谱使我们能够对许多此前仅大致界定的标记进行排序,并排除了分配到该区域的23个假定候选基因。我们发现OPA1关键区间为450 - 550 kb。它包含2个已知基因,即RPL35a和SDHA,因此这两个基因构成了候选基因。

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