Rogina B, Coelho C N, Kosher R A, Upholt W B
Department of BioStructure and Function, School of Dental Medicine, University of Connecticut Health Center, Farmington 06030.
Dev Dyn. 1992 Jan;193(1):92-101. doi: 10.1002/aja.1001930112.
Homeobox-containing genes have been implicated in a variety of patterning events during vertebrate limb development. In an attempt to isolate cDNAs corresponding to 5' members of the chicken HOX 4 cluster of homeobox-containing genes, a cDNA library constructed from mRNAs expressed during early stages of chick limb development was screened with probes generated by the polymerase chain reaction (PCR) using oligonucleotide primers corresponding to sequences in the homeoboxes of the human HOX4C and HOX4F genes, the human homologs of Hox-4.4 and Hox-4.6. This screening resulted in the isolation of full length cDNAs for the chicken homolog of HOX4F (cognate of mouse Hox-4.6), which we have termed GHox-4.6, and the chicken homolog of human HOX1I, which we have named GHox-1i, a paralog of Hox-4.6 in the HOX 1 cluster. The homeodomains encoded by GHox-4.6 and GHox-1i differ by only three amino acids, and the two proteins show extensive similarity along their entire lengths. Despite their sequence similarity, in situ hybridization analysis has revealed that GHox-4.6 and GHox-1i exhibit strikingly different spatial patterns of expression during embryonic chick limb development. At early stages of limb development (stages 20-22), GHox-4.6 transcripts are present in high amounts throughout the posterior half of the limb mesoderm and are absent from the anterior half of the mesoderm, an expression pattern consistent with the possible involvement of GHox-4.6 in the specification of posterior positional identity. In contrast, GHox-1i exhibits no distinct anterior-posterior polarity of expression at stage 22, but rather is expressed in high amounts throughout the mesenchyme of the limb bud. At later stages of development (stage 25), GHox-1i continues to be expressed in high amounts throughout the undifferentiated mesenchyme subjacent to the apical ectodermal ridge, and, in addition, is expressed in the mesodermal cells in the proximal peripheral regions of the limb bud subjacent to the ectoderm which are differentiating into nonchondrogenic lineages. Conversely, little or no expression of GHox-1i is detectable in the proximal central core of the limb bud where chondrogenic differentiation is occurring. Thus, GHox-1i is expressed by the undifferentiated subridge mesenchymal cells and proximal peripheral mesenchymal cells of the limb bud that are being inhibited from undergoing chondrogenesis by the apical ectodermal ridge and nonridge ectoderm.(ABSTRACT TRUNCATED AT 400 WORDS)
含同源框基因与脊椎动物肢体发育过程中的多种模式形成事件有关。为了分离与鸡HOX 4含同源框基因簇5'端成员相对应的cDNA,我们用聚合酶链反应(PCR)生成的探针筛选了一个由鸡胚肢体发育早期阶段表达的mRNA构建的cDNA文库,该探针使用的寡核苷酸引物对应于人类HOX4C和HOX4F基因同源框中的序列,它们分别是Hox-4.4和Hox-4.6的人类同源物。这次筛选分离出了HOX4F鸡同源物(小鼠Hox-4.6的同源物)的全长cDNA,我们将其命名为GHox-4.6,以及人类HOX1I的鸡同源物,我们将其命名为GHox-1i,它是HOX 1簇中Hox-4.6的旁系同源物。GHox-4.6和GHox-1i编码的同源结构域仅相差三个氨基酸,并且这两种蛋白质在其全长上显示出广泛的相似性。尽管它们的序列相似,但原位杂交分析表明,GHox-4.6和GHox-1i在鸡胚肢体发育过程中表现出截然不同的空间表达模式。在肢体发育的早期阶段(第20 - 22阶段),GHox-4.6转录本大量存在于肢体中胚层后半部分,而在前半部分中胚层中不存在,这种表达模式与GHox-4.6可能参与确定后部位置身份一致。相反,GHox-1i在第22阶段没有明显的前后极性表达,而是在整个肢芽间充质中大量表达。在发育的后期阶段(第25阶段),GHox-1i继续在顶端外胚层嵴下方的未分化间充质中大量表达,此外,在肢芽近端周边区域外胚层下方正在分化为非软骨形成谱系的中胚层细胞中也有表达。相反,在肢芽近端中央核心区域,即正在发生软骨形成分化的区域,几乎检测不到GHox-1i的表达。因此,GHox-1i由肢芽的未分化嵴下间充质细胞和近端周边间充质细胞表达,这些细胞受到顶端外胚层嵴和非嵴外胚层的抑制而无法进行软骨形成。(摘要截断于400字)