人l型丙酮酸激酶(PKLR)和葡萄糖脑苷酶(GBA)基因区域的结构和连锁关系

A Demina, E Boas, E Beutler
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摘要

l型丙酮酸激酶基因(PKLR)和糖脑苷酶(GBA)基因均位于人类1号染色体q21带上。鉴定和定位了两个重叠的P1噬菌体克隆,其中包含plklr和GBA,确定了这两个基因以及GBA假基因(psi GBA) metaxin (MTX), MTX假基因(psi MTX)和血栓反应蛋白3 (THBS3)的位置。测定了GBA与plklr的5′端距离为71 kb。PKLR基因的转录方向与GBA基因的转录方向趋同。所有195例高谢病患者均为1226G突变纯合,代表390条1226G突变染色体,具有PvuII -/- GBA单倍型和PKLR基因nt 1705处的C/C(-/-单倍型)。所有56例1226G/84GG复合杂合子的戈谢病患者均表现为-/+ GBA单倍型,56例患者中有55例PKLR nt 1705为-/+。只有1例1226G/84GG基因型患者与PKLR多态性出现交叉,在nt 1705处出现-/-单倍型。同样,9例PKLR 1529A/1529A基因型的丙酮酸激酶缺陷患者均具有相同的-/- GBA单倍型。
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Structure and linkage relationships of the region containing the human L-type pyruvate kinase (PKLR) and glucocerebrosidase (GBA) genes.

Both the L-type pyruvate kinase gene (PKLR) and glucocerebrosidase (GBA) gene are on band q21 of chromosome 1 in humans. Two overlapping P1 bacteriophage clones containing PKLR and GBA were identified and mapped, defining the locations of these two genes as well as those of the GBA pseudogene (psi GBA) metaxin (MTX), the MTX pseudogene (psi MTX), and thrombospondin 3 (THBS3). The distance between the 5' ends of GBA and PKLR was determined to be 71 kb. The direction of transcription PKLR gene was convergent to that of the GBA gene. All 195 Gaucher disease patients homozygous for the 1226G mutation, representing 390 chromosomes with the 1226G mutation, had a PvuII -/- GBA haplotype and a C/C at nt 1705 of the PKLR gene (-/- haplotype). All 56 Gaucher disease patients who were 1226G/84GG compound heterozygotes manifested a -/+ GBA haplotype and 55 of 56 patients were -/+ at PKLR nt 1705. Only 1 patient with 1226G/84GG genotype showed a crossover with the PKLR polymorphism, with a -/- haplotype at nt 1705. Similarly, 9 patients deficient in pyruvate kinase with the PKLR 1529A/1529A genotype were all found to have the same -/- GBA haplotype.

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