Harfe Brian D, McManus Michael T, Mansfield Jennifer H, Hornstein Eran, Tabin Clifford J
Department of Molecular Genetics and Microbiology, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Proc Natl Acad Sci U S A. 2005 Aug 2;102(31):10898-903. doi: 10.1073/pnas.0504834102. Epub 2005 Jul 22.
The RNaseIII-containing enzyme Dicer is believed to be required for the processing of most, if not all, microRNAs (miRNAs) and for processing long dsRNA into small interfering RNAs. Because the complete loss of Dicer in both zebrafish and mice results in early embryonic lethality, it has been impossible to determine what role, if any, Dicer has in patterning later tissues in the developing vertebrate embryo. To bypass the early requirement of Dicer in development, we have created a conditional allele of this gene in mice. Using transgenes to drive Cre expression in discrete regions of the limb mesoderm, we find that removal of Dicer results in the loss of processed miRNAs. Phenotypically, developmental delays, in part due to massive cell death as well as disregulation of specific gene expression, lead to the formation of a much smaller limb. Thus, Dicer is required for the formation of normal mouse limbs. Strikingly, however, we did not detect defects in basic patterning or in tissue-specific differentiation of Dicer-deficient limb buds.
含核糖核酸酶III的酶Dicer被认为是处理大多数(即便不是全部)微小RNA(miRNA)以及将长双链RNA加工成小干扰RNA所必需的。由于斑马鱼和小鼠体内Dicer的完全缺失会导致早期胚胎致死,因此一直无法确定Dicer在发育中的脊椎动物胚胎后期组织形成中是否发挥作用(若有作用,作用是什么)。为了绕过发育过程中对Dicer的早期需求,我们在小鼠中创建了该基因的条件等位基因。利用转基因在肢体中胚层的离散区域驱动Cre表达,我们发现去除Dicer会导致加工后的miRNA缺失。从表型上看,发育延迟部分是由于大量细胞死亡以及特定基因表达失调,导致形成的肢体要小得多。因此,Dicer是正常小鼠肢体形成所必需的。然而,令人惊讶的是,我们未在Dicer缺陷肢体芽的基本模式形成或组织特异性分化中检测到缺陷。