McGlinn Edwina, Yekta Soraya, Mansfield Jennifer H, Soutschek Jürgen, Bartel David P, Tabin Clifford J
Department of Genetics, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2009 Nov 3;106(44):18610-5. doi: 10.1073/pnas.0910374106. Epub 2009 Oct 21.
Patterning of the vertebrate axial skeleton requires precise spatial and temporal control of Hox gene expression during embryonic development. MicroRNAs (miRNAs) are recently described modulators of gene activity, and members of the miR-196 and miR-10 families have been shown to target several Hox genes in vivo. Testing miRNA function in mice is complicated by potential redundancy between family members. To circumvent this, we have developed protocols for introducing modified antisense oligonucleotides (antagomiRs) in ovo during chick development. Using this approach, we identify a layer of regulatory control provided by the miR-196 family in defining the boundary of Hox gene expression along the anterior-posterior (A-P) embryonic axis. Following knockdown of miR-196, we observe a homeotic transformation of the last cervical vertebrae toward a thoracic identity. This phenotypic alteration is, in part, due to an anterior expansion of Hoxb8 gene expression and consolidates the in vivo relevance of post-transcriptional Hox gene regulation provided by miRNAs in the complex hierarchies governing axial pattering.
脊椎动物轴骨骼的模式形成需要在胚胎发育过程中对Hox基因表达进行精确的空间和时间控制。微小RNA(miRNA)是最近被描述的基因活性调节剂,并且已证明miR-196和miR-10家族的成员在体内靶向多个Hox基因。由于家族成员之间存在潜在的冗余性,在小鼠中测试miRNA功能变得复杂。为了规避这一问题,我们开发了在鸡胚发育过程中在卵内引入修饰的反义寡核苷酸(抗miR)的方案。使用这种方法,我们确定了miR-196家族在沿前后(A-P)胚胎轴定义Hox基因表达边界方面提供的一层调控控制。在敲低miR-196后,我们观察到最后一个颈椎向胸椎身份的同源异型转化。这种表型改变部分是由于Hoxb8基因表达的向前扩展,并巩固了miRNA在控制轴模式形成的复杂层次结构中提供的转录后Hox基因调控在体内的相关性。