Charmley P, Concannon P, Hood L, Rowen L
Virginia Mason Research Center, Seattle, Washington 98101, USA.
Genomics. 1995 Oct 10;29(3):760-5. doi: 10.1006/geno.1995.9940.
The human T-cell receptor beta-chain (TCRB) gene complex spans 575 kb in chromosome region 7q35 and has been the subject of a large-scale DNA sequencing effort. A contiguous 685-kb DNA sequence from this region was searched by computer analysis for the occurrence of simple sequence repeats (microsatellites) with core sequence lengths of 2-5 nucleotides. Twenty-nine such microsatellites of repeat number n > or = 9 were found, with the majority being dinucleotide repeats. By PCR analysis, 19 were found to be polymorphic in repeat number, thus averaging one per 36 kb. These polymorphic di-, tri-, and tetranucleotide repeats had between 3 and 15 differently sized alleles each. The potential usefulness of these TCRB microsatellites for detecting disease susceptibility alleles was examined by measuring the linkage disequilibrium between these markers and flanking biallelic mutations. All but 4 microsatellites (79%) demonstrated significant linkage disequilibrium (P < 0.0001). This present study highlights the utility and potential outcomes of large-scale DNA sequencing for the identification of polymorphic simple sequence repeats.
人类T细胞受体β链(TCRB)基因复合体位于7号染色体区域7q35,跨度为575 kb,并且一直是大规模DNA测序工作的研究对象。通过计算机分析,在该区域一段连续的685 kb DNA序列中搜索核心序列长度为2至5个核苷酸的简单序列重复(微卫星)。发现了29个重复数n≥9的此类微卫星,其中大多数是二核苷酸重复。通过PCR分析,发现其中19个在重复数上具有多态性,因此平均每36 kb有一个。这些多态性二核苷酸、三核苷酸和四核苷酸重复序列各自具有3至15个不同大小的等位基因。通过测量这些标记与侧翼双等位基因突变之间的连锁不平衡,研究了这些TCRB微卫星在检测疾病易感性等位基因方面的潜在用途。除4个微卫星外(79%),所有微卫星均表现出显著的连锁不平衡(P<0.0001)。本研究突出了大规模DNA测序在鉴定多态性简单序列重复方面的实用性和潜在成果。