Magenis R E, Donlon T A, Tomar D R
Hum Genet. 1985;69(4):300-3. doi: 10.1007/BF00291645.
Chromosome preparations from four subjects, one normal 46,XY male and three patients with different rearrangements of chromosome 11: 46,XX,del(11)(p11.2----p15.1), 46,XY,inv(11)(p13q24.2), and 46,XY,rec(11)inv(11)(p13q24.2) pat, were utilized for in situ hybridization studies with a tritium-labeled cDNA probe containing a beta-globin insert. Using the hybridization technique described by Harper and Saunders (1981), there were 1-2 grains over each labeled metaphase. Of 360 cells scored, 88 were labeled over chromosome 11, band p15 (24%). Approximately half of the chromosome 11s labeled from the abnormal patients were the del(11) or inv(11). These results exclude the beta-globin locus from 11p11----p14, since these bands were not present in the deleted 11, and assign it to 11p15. This is in agreement with the recent exclusion data of de Martinville and Francke (1984) and Junien (1984), and suggestive assignment data of Morton et al. (1984).
对四名受试者的染色体标本进行了研究,其中一名是正常的46,XY男性,另外三名是11号染色体有不同重排的患者:46,XX,del(11)(p11.2----p15.1)、46,XY,inv(11)(p13q24.2)和46,XY,rec(11)inv(11)(p13q24.2) pat,使用含有β-珠蛋白插入片段的氚标记cDNA探针进行原位杂交研究。采用Harper和Saunders(1981年)描述的杂交技术,每个标记的中期相上有1至2个银粒。在计数的360个细胞中,有88个在11号染色体p15带处被标记(24%)。来自异常患者的被标记的11号染色体中,约一半是del(11)或inv(11)。这些结果将β-珠蛋白基因座排除在11p11----p14之外,因为这些带在缺失的11号染色体中不存在,并将其定位到11p15。这与de Martinville和Francke(1984年)以及Junien(1984年)最近的排除数据以及Morton等人(1984年)的推测定位数据一致。