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Hox A11 突变小鼠的同源异型转化和肢体缺陷

Homeotic transformations and limb defects in Hox A11 mutant mice.

作者信息

Small K M, Potter S S

机构信息

Division of Basic Science Research, Children's Hospital Research Foundation, Cincinnati, Ohio 45229.

出版信息

Genes Dev. 1993 Dec;7(12A):2318-28. doi: 10.1101/gad.7.12a.2318.

Abstract

Hox A11 is one of the expanded set of vertebrate homeo box (Hox) genes with similarities to the Drosophila homeotic gene, Abdominal-B (Abd-B). These Abd-B-type Hox genes have been shown to be expressed in the most caudal regions of the developing vertebrate embryo and in overlapping domains within the developing limbs, suggesting that these genes play important roles in pattern formation in both appendicular and axial regions of the body. In this report whole-mount in situ hybridization in mouse embryos gave a precise description of Hox A11 gene expression in the developing limbs and in the axial domain of the developing body. In addition, we generated a targeted mutation in Hox A11 and characterized the resulting phenotype to begin to dissect developmental functions of the Abd-B subfamily of Hox genes. Hox A11 mutant mice exhibited double homeotic transformations, with the thirteenth thoracic segment posteriorized to form an additional first lumbar vertebra and with the sacral region anteriorized, generating yet another lumbar segment. Furthermore, skeletal malformations were observed in both forelimbs and hindlimbs. In mutant forelimbs, the ulna and radius were misshapen, the pisiform and triangular carpal bones were fused, and abnormal sesamoid bone development occurred. In mutant hindlimbs the tibia and fibula were joined incorrectly and malformed at their distal ends. Also, an enlarged sesamoid developed ventral to the tibiale bone. Both heterozygous and homozygous mice displayed mutant phenotypes adding an additional level of complexity to the Hox code hypothesis.

摘要

Hox A11是脊椎动物同源框(Hox)基因扩展集中的一员,与果蝇同源异型基因腹B(Abd - B)相似。这些Abd - B型Hox基因已被证明在发育中的脊椎动物胚胎的最尾端区域以及发育中的肢体的重叠区域表达,这表明这些基因在身体的附属和轴向区域的模式形成中发挥重要作用。在本报告中,对小鼠胚胎进行的全胚胎原位杂交精确描述了Hox A11基因在发育中的肢体和发育中身体的轴向区域的表达。此外,我们在Hox A11中产生了靶向突变,并对由此产生的表型进行了表征,以开始剖析Hox基因Abd - B亚家族的发育功能。Hox A11突变小鼠表现出双重同源异型转变,第十三胸段向后化形成额外的第一腰椎,骶骨区域向前化,产生另一个腰椎段。此外,在前肢和后肢均观察到骨骼畸形。在突变前肢中,尺骨和桡骨畸形,豌豆骨和三角腕骨融合,并且籽骨发育异常。在突变后肢中,胫骨和腓骨连接错误且远端畸形。此外,在胫骨骨腹侧出现一个增大的籽骨。杂合子和纯合子小鼠均表现出突变表型,这为Hox编码假说增加了额外的复杂性。

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