Diabetes Center, University of California San Francisco, San Francisco, California 94143, USA.
Nature. 2010 Feb 11;463(7282):775-80. doi: 10.1038/nature08748.
Insulin from the beta-cells of the pancreatic islets of Langerhans controls energy homeostasis in vertebrates, and its deficiency causes diabetes mellitus. During embryonic development, the transcription factor neurogenin 3 (Neurog3) initiates the differentiation of the beta-cells and other islet cell types from pancreatic endoderm, but the genetic program that subsequently completes this differentiation remains incompletely understood. Here we show that the transcription factor Rfx6 directs islet cell differentiation downstream of Neurog3. Mice lacking Rfx6 failed to generate any of the normal islet cell types except for pancreatic-polypeptide-producing cells. In human infants with a similar autosomal recessive syndrome of neonatal diabetes, genetic mapping and subsequent sequencing identified mutations in the human RFX6 gene. These studies demonstrate a unique position for Rfx6 in the hierarchy of factors that coordinate pancreatic islet development in both mice and humans. Rfx6 could prove useful in efforts to generate beta-cells for patients with diabetes.
胰岛β细胞分泌的胰岛素控制着脊椎动物的能量稳态,其缺乏会导致糖尿病。在胚胎发育过程中,转录因子神经基因 3(Neurog3)启动了胰岛β细胞和其他胰岛细胞类型从胰腺内胚层的分化,但随后完成这种分化的遗传程序仍不完全清楚。在这里,我们表明转录因子 Rfx6 指导 Neurog3 下游的胰岛细胞分化。缺乏 Rfx6 的小鼠未能产生任何正常的胰岛细胞类型,除了产生胰多肽的细胞。在具有类似常染色体隐性遗传新生儿糖尿病的人类婴儿中,通过遗传图谱和随后的测序鉴定了人类 RFX6 基因的突变。这些研究表明 Rfx6 在协调小鼠和人类胰腺胰岛发育的因子层次中具有独特的地位。Rfx6 可能有助于为糖尿病患者生成β细胞。