Simeone A, Acampora D, Pannese M, D'Esposito M, Stornaiuolo A, Gulisano M, Mallamaci A, Kastury K, Druck T, Huebner K
International Institute of Genetics and Biophysics, Consiglio Nazionale delle Ricerche, Naples, Italy.
Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2250-4. doi: 10.1073/pnas.91.6.2250.
A number of vertebrate genes of the Dlx gene family have been cloned in mouse, frog, and zebrafish. These genes contain a homeobox related to that of Distalless, a gene expressed in the developing head and limbs of Drosophila embryos. We cloned and studied the expression of two members of this family, which we named Dlx5 and Dlx6, in human and mouse. The two human genes, DLX5 and DLX6, are closely linked in an inverted convergent configuration in a region of chromosome 7, at 7q22. Similarly, the two human genes DLX1 and DLX2 are closely linked in a convergent configuration at 2q32, near the HOXD (previously HOX4) locus. In situ hybridization experiments in mouse embryos revealed expression of Dlx5 and Dlx6 mRNA in restricted regions of ventral diencephalon and basal telencephalon, with a distribution very similar to that reported for Dlx1 and Dlx2 mRNA. A surprising feature of Dlx5 and Dlx6 is that they are also expressed in all skeletal structures of midgestation embryos after the first cartilage formation. The expression pattern of these genes, together with their chromosome localization, may provide useful cues for the study of congenital disorders in which there is a combination of craniofacial and limb defects.
Dlx基因家族的许多脊椎动物基因已在小鼠、青蛙和斑马鱼中克隆出来。这些基因含有一个与Distalless相关的同源异型框,Distalless是一种在果蝇胚胎发育中的头部和四肢表达的基因。我们克隆并研究了该家族的两个成员,我们将其命名为Dlx5和Dlx6,在人类和小鼠中的表达情况。两个人类基因DLX5和DLX6在7号染色体7q22区域以反向汇聚的形式紧密相连。同样,两个人类基因DLX1和DLX2在2q32区域以汇聚的形式紧密相连,靠近HOXD(以前的HOX4)基因座。对小鼠胚胎进行的原位杂交实验显示,Dlx5和Dlx6 mRNA在腹侧间脑和基底前脑的特定区域表达,其分布与报道的Dlx1和Dlx2 mRNA的分布非常相似。Dlx5和Dlx6的一个惊人特征是,它们在第一次软骨形成后的妊娠中期胚胎的所有骨骼结构中也有表达。这些基因的表达模式及其染色体定位,可能为研究同时存在颅面和肢体缺陷的先天性疾病提供有用线索。