Chen Yingwei, Sagar Vatsala, Len Hoay-Shuen, Peterson Katherine, Fan Jianguo, Mishra Sanghamitra, McMurtry John, Wilmarth Phillip A, David Larry L, Wistow Graeme
Section on Molecular Structure and Functional Genomics, National Eye Institute, National Institutes of Health, Bethesda, MD, USA.
USDA, ARS, Southern Plains Area, East College Station, TX, USA.
FEBS J. 2016 Apr;283(8):1516-30. doi: 10.1111/febs.13689. Epub 2016 Mar 11.
γ-Crystallins, abundant proteins of vertebrate lenses, were thought to be absent from birds. However, bird genomes contain well-conserved genes for γS- and γN-crystallins. Although expressed sequence tag analysis of chicken eye found no transcripts for these genes, RT-PCR detected spliced transcripts for both genes in chicken lens, with lower levels in cornea and retina/retinal pigment epithelium. The level of mRNA for γS in chicken lens was relatively very low even though the chicken crygs gene promoter had lens-preferred activity similar to that of mouse. Chicken γS was detected by a peptide antibody in lens, but not in other ocular tissues. Low levels of γS and γN proteins were detected in chicken lens by shotgun mass spectroscopy. Water-soluble and water-insoluble lens fractions were analyzed and 1934 proteins (< 1% false discovery rate) were detected, increasing the known chicken lens proteome 30-fold. Although chicken γS is well conserved in protein sequence, it has one notable difference in leucine 16, replacing a surface glutamine conserved in other γ-crystallins, possibly affecting solubility. However, L16 and engineered Q16 versions were both highly soluble and had indistinguishable circular dichroism, tryptophan fluorescence and heat stability (melting temperature Tm ~ 65 °C) profiles. L16 has been present in birds for over 100 million years and may have been adopted for a specific protein interaction in the bird lens. However, evolution has clearly reduced or eliminated expression of ancestral γ-crystallins in bird lenses. The conservation of genes for γS- and γN-crystallins suggests they may have been preserved for reasons unrelated to the bulk properties of the lens.
γ-晶状体蛋白是脊椎动物晶状体中丰富的蛋白质,过去认为鸟类体内不存在这种蛋白。然而,鸟类基因组中含有γS-和γN-晶状体蛋白的保守基因。尽管对鸡眼睛的表达序列标签分析未发现这些基因的转录本,但逆转录聚合酶链反应(RT-PCR)检测到鸡晶状体中这两个基因的剪接转录本,在角膜和视网膜/视网膜色素上皮中的水平较低。尽管鸡crygs基因启动子具有与小鼠相似的晶状体偏好活性,但鸡晶状体中γS的mRNA水平相对非常低。用肽抗体在晶状体中检测到了鸡γS,但在其他眼组织中未检测到。通过鸟枪法质谱在鸡晶状体中检测到低水平的γS和γN蛋白。对水溶性和水不溶性晶状体组分进行了分析,检测到1934种蛋白质(错误发现率<1%),使已知的鸡晶状体蛋白质组增加了30倍。尽管鸡γS在蛋白质序列上高度保守,但它在第16位亮氨酸上有一个显著差异,取代了其他γ-晶状体蛋白中保守的表面谷氨酰胺,这可能会影响溶解性。然而,L16和工程化的Q16版本都具有高度溶解性,并且在圆二色性、色氨酸荧光和热稳定性(熔解温度Tm~65°C)方面的图谱无法区分。L16在鸟类中已经存在了超过1亿年,可能已被用于鸟类晶状体中的特定蛋白质相互作用。然而,进化显然已经减少或消除了鸟类晶状体中祖先γ-晶状体蛋白的表达。γS-和γN-晶状体蛋白基因的保守性表明,它们可能是出于与晶状体整体特性无关的原因而被保留下来的。