Blin N, Müllenbach R, Suijkerbuijk R, Herzog R, Meese E
Institut für Anthropologie and Humangenetik, Univ. Tübingen, Germany.
Cancer Genet Cytogenet. 1993 Oct 15;70(2):108-11. doi: 10.1016/0165-4608(93)90177-n.
Many human meningiomas show loss of heterozygosity at distal loci but retain constitutional heterozygosity at one or more proximal loci of 22q. Molecular analysis indicted deletions involving at least the region 22q12.3-qter. In this region, distal to myoglobin, the putative meningioma locus ought to be expected. Long-range mapping was performed around two loci from 22q12.3-q13.1 (D22S16 and PDGFB, the most proximal locus to be lost in meningioma). D22S16, originally assigned to 22q13-qter by isotopic in situ hybridization, was placed in the vicinity of PDGFB by utilizing a set of somatic cell hybrids, an assignment confirmed by fluorescence in situ hybridization (FISH) of a cosmid clone containing the D22S16 locus. Moreover, pulsed field gel electrophoresis suggests a close linkage of both markers within 630 kb.
许多人类脑膜瘤在远端位点显示杂合性缺失,但在22q的一个或多个近端位点保留了组成型杂合性。分子分析表明缺失至少涉及22q12.3-qter区域。在该区域,肌红蛋白远端,应该预期存在推定的脑膜瘤位点。围绕22q12.3-q13.1的两个位点(D22S16和PDGFB,脑膜瘤中最近端的丢失位点)进行了长距离定位。D22S16最初通过同位素原位杂交定位到22q13-qter,通过利用一组体细胞杂种将其置于PDGFB附近,包含D22S16位点的粘粒克隆的荧光原位杂交(FISH)证实了这一定位。此外,脉冲场凝胶电泳表明两个标记在630 kb内紧密连锁。