Zhang J, Qiao J, Song W, Qiu Z
Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, School of Basic Medicine, Peking Union Medical College, Beijing, China.
Sci China C Life Sci. 1996 Jun;39(3):329-36.
A permanent lymphocyte cell line of a heterozygote with Yunnanese (A gamma delta beta)0-thalassemia deletion, associated with an increased production of G gamma globin in adult, was founded using Epstein-Barr virus transformation. The hybrids of the lymphocyte cell and mouse erythroleukemia cell (MEL) were achieved and the hybrids containing human chromosome 11 were selected with the monoclonal antibody 53/6. The subclones containing only either the normal or the abnormal human chromosome 11 were separated and the expression of the human globin genes was studied. Expression of the beta-globin gene, but not the G gamma and A gamma, was observed in the hybrids containing only the normal human chromosome 11, while active expression of the G gamma globin gene was observed in the hybrids containing only the abnormal human chromosome 11. These results have confirmed that the DNA deletion in the beta-globin gene cluster is the cause of persistent active expression of the G gamma globin gene in the Yunnanese mutant.
利用爱泼斯坦-巴尔病毒转化技术,建立了一株携带云南(Aγδβ)0-地中海贫血缺失的杂合子永久性淋巴细胞系,该杂合子在成人中Gγ珠蛋白产量增加。获得了淋巴细胞与小鼠红白血病细胞(MEL)的杂交细胞,并使用单克隆抗体53/6筛选出含有人类11号染色体的杂交细胞。分离出仅含有正常或异常人类11号染色体的亚克隆,并研究了人类珠蛋白基因的表达。在仅含有正常人类11号染色体的杂交细胞中观察到β-珠蛋白基因的表达,但未观察到Gγ和Aγ珠蛋白基因的表达,而在仅含有异常人类11号染色体的杂交细胞中观察到Gγ珠蛋白基因的活跃表达。这些结果证实,β-珠蛋白基因簇中的DNA缺失是云南突变体中Gγ珠蛋白基因持续活跃表达的原因。