Gerido Dwan A, Sellitto Caterina, Li Leping, White Thomas W
Department of Physiology and Biophysics, State University of New York, Stony Brook, New York 11794-8661, USA.
Invest Ophthalmol Vis Sci. 2003 Jun;44(6):2669-74. doi: 10.1167/iovs.02-1311.
Deletion of connexin (Cx)50 produces microphthalmia with nuclear cataracts. To determine whether these two traits are influenced by genetic background and are dependent on each other, mice carrying the Cx50 deletion in two different strains were generated, and the growth defect and severity of cataracts were analyzed.
Cx50-knockout mice were generated in the 129S6 strain, and back-crossed into the C57BL/6J genetic background. To analyze the influence of genetic background on the observed phenotype, postnatal lens growth, lens clarity, lens histology and crystallin solubility were determined and compared between the two strains of Cx50-knockout mice.
The growth deficiency persisted, regardless of genetic background, but genetic modifiers that differentially altered the solubility of crystallin proteins influenced the severity of cataracts. Expression levels of Cx46 were similar in all animals, regardless of genetic background, indicating that the differences were not due to a compensatory upregulation of Cx46.
Taken together, these data indicate that the two components of the Cx50 phenotype are independent of each other and that cataractogenesis is under the influence of an unidentified genetic modifier.
连接蛋白(Cx)50缺失会导致小眼球合并核性白内障。为了确定这两个特征是否受遗传背景影响以及是否相互依赖,我们培育了在两种不同品系中携带Cx50缺失的小鼠,并分析了其生长缺陷和白内障严重程度。
在129S6品系中培育Cx50基因敲除小鼠,并回交到C57BL/6J遗传背景。为了分析遗传背景对观察到的表型的影响,我们测定并比较了两种Cx50基因敲除小鼠品系之间的出生后晶状体生长、晶状体透明度、晶状体组织学和晶状体蛋白溶解度。
无论遗传背景如何,生长缺陷均持续存在,但不同改变晶状体蛋白溶解度的遗传修饰因子影响了白内障的严重程度。无论遗传背景如何,所有动物中Cx46的表达水平相似,这表明差异并非由于Cx46的代偿性上调所致。
综上所述,这些数据表明Cx50表型的两个组成部分相互独立,并且白内障的发生受一个未明确的遗传修饰因子影响。