Gendron-Maguire M, Mallo M, Zhang M, Gridley T
Roche Institute of Molecular Biology, Roche Research Center, Nutley, New Jersey 07110.
Cell. 1993 Dec 31;75(7):1317-31. doi: 10.1016/0092-8674(93)90619-2.
Mice homozygous for a targeted mutation of the Hoxa-2 (Hox 1.11) gene are born with cleft palates and die within 24 hr of birth. Analysis of stained skeletons revealed that homozygous mutant animals contained multiple cranial skeletal defects, including a duplication of the ossification centers of the bones of the middle ear. Histological analysis suggested that this duplication resulted from the transformation of skeletal elements derived from the second branchial arch into more anterior structures, resulting in a duplication of Meckel's cartilage adjacent to the otic capsule. Skeletal elements normally derived from the second arch were absent in the mutants. These data provide direct experimental evidence for the existence of a branchial Hox code.
Hoxa-2(Hox 1.11)基因靶向突变的纯合小鼠出生时伴有腭裂,并在出生后24小时内死亡。对染色骨骼的分析显示,纯合突变动物存在多种颅骨骨骼缺陷,包括中耳骨化中心的重复。组织学分析表明,这种重复是由于源自第二鳃弓的骨骼元素转化为更靠前的结构,导致耳囊附近的梅克尔软骨重复。突变体中通常源自第二鳃弓的骨骼元素缺失。这些数据为鳃Hox密码的存在提供了直接的实验证据。