Rodman D M, Zamudio S
Division of Pulmonary Sciences, University of Colorado Health Sciences Center, Denver 80262.
Med Hypotheses. 1991 Nov;36(3):253-8. doi: 10.1016/0306-9877(91)90144-n.
Cystic fibrosis (CF) is the most common fatal genetic disorder of caucasians. While it has been hypothesized that there is a CF heterozygote advantage which allowed the gene to achieve such high prevalence, the nature of that advantage remains a mystery. The recent identification and sequencing of the CF gene has increased the probability that the CF heterozygote advantage will be discovered. In this hypothesis we review the information which is known about the selection of the CF mutation and its cellular consequences, and present evidence which suggests that resistance to cholera may have been the environmental factor which selected CF heterozygotes over their 'normal' homozygote cohort. Future lines of experimentation and possible clinical applicability to therapy of secretory diarrhea are presented.
囊性纤维化(CF)是白种人中最常见的致命性遗传疾病。尽管有人提出假说认为存在CF杂合子优势,使得该基因能够达到如此高的流行率,但其优势的本质仍是个谜。CF基因的近期鉴定和测序增加了发现CF杂合子优势的可能性。在本假说中,我们回顾了关于CF突变选择及其细胞后果的已知信息,并提出证据表明对霍乱的抗性可能是在CF杂合子与其“正常”纯合子群体中选择CF杂合子的环境因素。还介绍了未来的实验方向以及对分泌性腹泻治疗可能的临床适用性。