German Research Center for Environmental Health, Institute of Developmental Genetics, Neuherberg, Germany.
PLoS One. 2011;6(8):e23678. doi: 10.1371/journal.pone.0023678. Epub 2011 Aug 17.
Fibroblast growth factor (Fgf) signalling plays a crucial role in many developmental processes. Among the Fgf pathway ligands, Fgf9 (UniProt: P54130) has been demonstrated to participate in maturation of various organs and tissues including skeleton, testes, lung, heart, and eye. Here we establish a novel Fgf9 allele, discovered in a dominant N-ethyl-N-nitrosourea (ENU) screen for eye-size abnormalities using the optical low coherence interferometry technique. The underlying mouse mutant line Aca12 was originally identified because of its significantly reduced lens thickness. Linkage studies located Aca12 to chromosome 14 within a 3.6 Mb spanning interval containing the positional candidate genes Fgf9 (MGI: 104723), Gja3 (MGI: 95714), and Ift88 (MGI: 98715). While no sequence differences were found in Gja3 and Ift88, we identified an A→G missense mutation at cDNA position 770 of the Fgf9 gene leading to an Y162C amino acid exchange. In contrast to previously described Fgf9 mutants, Fgf9(Y162C) carriers were fully viable and did not reveal reduced body-size, male-to-female sexual reversal or skeletal malformations. The histological analysis of the retina as well as its basic functional characterization by electroretinography (ERG) did not show any abnormality. However, the analysis of head-tracking response of the Fgf9(Y162C) mutants in a virtual drum indicated a gene-dosage dependent vision loss of almost 50%. The smaller lenses in Fgf9(Y162C) suggested a role of Fgf9 during lens development. Histological investigations showed that lens growth retardation starts during embryogenesis and continues after birth. Young Fgf9(Y162C) lenses remained transparent but developed age-related cataracts. Taken together, Fgf9(Y162C) is a novel neomorphic allele that initiates microphakia and reduced vision without effects on organs and tissues outside the eye. Our data point to a role of Fgf9 signalling in primary and secondary lens fiber cell growth. The results underline the importance of allelic series to fully understand multiple functions of a gene.
成纤维细胞生长因子(Fgf)信号在许多发育过程中起着至关重要的作用。在 Fgf 途径配体中,Fgf9(UniProt:P54130)已被证明参与包括骨骼、睾丸、肺、心脏和眼睛在内的各种器官和组织的成熟。在这里,我们建立了一个新的 Fgf9 等位基因,该基因是在使用光学低相干干涉测量技术进行的显性 N-乙基-N-亚硝脲(ENU)筛选眼部大小异常中发现的。最初发现的潜在小鼠突变系 Aca12 是因为其晶状体厚度显著减少而被识别的。连锁研究将 Aca12 定位在包含位置候选基因 Fgf9(MGI:104723)、Gja3(MGI:95714)和 Ift88(MGI:98715)的 3.6 Mb 跨度区间内的 14 号染色体上。虽然在 Gja3 和 Ift88 中没有发现序列差异,但我们在 Fgf9 基因的 cDNA 位置 770 处发现了一个 A→G 错义突变,导致 Y162C 氨基酸替换。与以前描述的 Fgf9 突变体不同,Fgf9(Y162C)携带者完全存活,并且没有表现出体型减小、雌雄间性逆转或骨骼畸形。视网膜的组织学分析以及通过视网膜电图(ERG)对其基本功能的特征描述均未显示任何异常。然而,在虚拟鼓中对头跟踪反应的分析表明,Fgf9(Y162C)突变体的基因剂量依赖性视力损失近 50%。Fgf9(Y162C)中的较小晶状体表明 Fgf9 在晶状体发育过程中的作用。组织学研究表明,晶状体生长迟缓始于胚胎发生期间,并在出生后继续。年轻的 Fgf9(Y162C)晶状体仍然透明,但会发展出与年龄相关的白内障。总之,Fgf9(Y162C)是一种新型的新等位基因,它会引发小眼球和视力下降,而不会对眼睛以外的器官和组织产生影响。我们的数据表明,Fgf9 信号在初级和次级晶状体纤维细胞生长中起作用。结果强调了等位基因系列对于充分理解一个基因的多种功能的重要性。