Andrews N C
Howard Hughes Medical Institute, Children's Hospital, Boston, Massachusetts 02115, USA.
Yale J Biol Med. 1997 May-Jun;70(3):219-26.
Iron is an essential nutrient, and disorders of iron metabolism are common. Nonetheless, intestinal iron absorption and cellular iron transport are poorly understood. Biochemical approaches to elucidating these processes have yielded little in the past decade. As an alternative approach, we have begun to study spontaneous mouse mutants, that have inherited defects in key steps in iron transport. We have undertaken positional cloning of the gene responsible for microcytic anemia (gene symbol mk). This report describes the important characteristics of these mice, and our progress in studying them.
铁是一种必需营养素,铁代谢紊乱很常见。然而,肠道铁吸收和细胞铁转运仍知之甚少。在过去十年中,用于阐明这些过程的生化方法收效甚微。作为一种替代方法,我们开始研究自发的小鼠突变体,这些突变体在铁转运的关键步骤中存在遗传缺陷。我们对导致小细胞性贫血的基因(基因符号为mk)进行了定位克隆。本报告描述了这些小鼠的重要特征以及我们在研究它们方面取得的进展。