To elucidate the morphological and cellular changes due to introduction of a charge during development and the possible mechanism that underlies cataract development in humans as a consequence of an additional charge, we generated a transgenic mouse model mimicking deamidation of Asn at position 101. The mouse model expresses a human ␣A-crystallin gene in which Asn-101 was replaced with Asp, which is referred to as ␣AN101D-transgene and is considered to be "deamidated" in this study. Mice expressing ␣AN101D-transgene are referred to here CRYAA N101D mice. All of the lines showed the expression of ␣AN101D-transgene. Compared with the lenses of mice expressing wild-type (WT) ␣A-transgene (referred to as CRYAA WT mice), the lenses of CRYAA N101D mice showed (a) altered ␣A-crystallin membrane protein (aquaporin-0 (AQP0), a specific lens membrane protein) interaction, (b) extracellular spaces between outer cortical fiber cells, (c) attenuated denucleation during confocal microscopic examination, (d) disrupted normal fiber cell organization and structure during scanning electron microscopic examination, (e) distorted posterior suture lines by bright field microscopy, and (f) development of a mild anterior lens opacity in the superior cortical region during the optical coherence tomography scan analysis. Relative to lenses with WT ␣A-crystallin, the lenses containing the deamidated ␣A-crystallin also showed an aggregation of ␣A-crystallin and a higher level of water-insoluble proteins, suggesting that the morphological and cellular changes in these lenses are due to the N101D mutation. This study provides evidence for the first time that expression of deamidated ␣A-crystallin caused disruption of fiber cell structural integrity, protein aggregation, insolubilization, and mild cortical lens opacity.The ocular lens has a unique cellular architecture consisting of a single layer of cuboidal epithelial cells, which divide and differentiate at the equator into fiber cells (1). The fiber cells elongate, and they synthesize fiber cell-specific proteins, such as AQP0 (aquaporin-0)/MIP (main intrinsic protein), cytoskeletal proteins, and crystallins (1-4). As the new fiber cells are laid down at the lens equator, the older fiber cells are pushed toward the lens core and simultaneously lose their nuclei and organelles while exhibiting very little protein turnover. Among the three classes of the vertebrate lens crystallins (␣-, -, and ␥-crystallins), ␣-crystallins are composed of two primary gene products, A and B, known as ␣A-and ␣B-crystallins, that show ϳ60% amino acid homology and constitute up to 50% of the total lens proteins. Both ␣A-and ␣B-crystallins belong to a family of small heat shock proteins with "chaperone" activity (5, 6). These crystallins are constitutively expressed in both lens epithelial and fiber cells (7) and undergo numerous age-related post-translational modifications (PTMs) 2 that lead to their unfolding, aggregation, and insolubilization. These PTMs eventually lead to accumulation of damaged crystal...