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Vision Res. 2011 Jan 28;51(2):269-79. doi: 10.1016/j.visres.2010.08.039. Epub 2010 Sep 6.
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The betagamma-crystallin superfamily contains a universal motif for binding calcium.β-晶状体蛋白超家族包含一个结合钙的通用基序。
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Isolation and characterization of betaA3-crystallin associated proteinase from alpha-crystallin fraction of human lenses.从人晶状体α-晶状体蛋白组分中分离并鉴定βA3-晶状体蛋白相关蛋白酶
Mol Vis. 2008;14:1872-85. Epub 2008 Oct 20.
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A novel non-lens betagamma-crystallin and trefoil factor complex from amphibian skin and its functional implications.一种来自两栖动物皮肤的新型非晶状体βγ-晶状体蛋白与三叶因子复合物及其功能意义。
PLoS One. 2008 Mar 12;3(3):e1770. doi: 10.1371/journal.pone.0001770.
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Near complete loss of retinal ganglion cells in the math5/brn3b double knockout elicits severe reductions of other cell types during retinal development.在math5/brn3b双基因敲除小鼠中,视网膜神经节细胞几乎完全丧失,这在视网膜发育过程中引发了其他细胞类型的严重减少。
Dev Biol. 2008 Apr 15;316(2):214-27. doi: 10.1016/j.ydbio.2008.01.015. Epub 2008 Jan 26.
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Changes in gene expression in experimental glaucoma and optic nerve transection: the equilibrium between protective and detrimental mechanisms.实验性青光眼和视神经横断中基因表达的变化:保护机制与有害机制之间的平衡
Invest Ophthalmol Vis Sci. 2007 Dec;48(12):5539-48. doi: 10.1167/iovs.07-0542.
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betaA3/A1-crystallin in astroglial cells regulates retinal vascular remodeling during development.星形胶质细胞中的βA3/A1-晶体蛋白在发育过程中调节视网膜血管重塑。
Mol Cell Neurosci. 2008 Jan;37(1):85-95. doi: 10.1016/j.mcn.2007.08.016. Epub 2007 Aug 31.
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Subfertility in mice harboring a mutation in betaB2-crystallin.携带βB2-晶体蛋白突变的小鼠的生育力低下。
Mol Vis. 2007 Mar 14;13:366-73.
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Modulation of alpha and beta crystallin expression in rat retinas with ocular hypertension-induced ganglion cell degeneration.眼压升高诱导大鼠视网膜神经节细胞变性时α和β晶状体蛋白表达的调节
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10
Elongation of axons during regeneration involves retinal crystallin beta b2 (crybb2).轴突再生过程中的延伸涉及视网膜βB2晶状体蛋白(crybb2)。
Mol Cell Proteomics. 2007 May;6(5):895-907. doi: 10.1074/mcp.M600245-MCP200. Epub 2007 Jan 29.

βA3/A1- 晶体蛋白在发育中和成年大鼠眼内的表达。

Expression of βA3/A1-crystallin in the developing and adult rat eye.

机构信息

Wilmer Eye Institute, The Johns Hopkins University School of Medicine, 400 N. Broadway, Smith Research Building, M035, Baltimore, MD 21287, USA.

出版信息

J Mol Histol. 2011 Feb;42(1):59-69. doi: 10.1007/s10735-010-9307-1. Epub 2011 Jan 4.

DOI:10.1007/s10735-010-9307-1
PMID:21203897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3840502/
Abstract

Crystallins are very abundant structural proteins of the lens and are also expressed in other tissues. We have previously reported a spontaneous mutation in the rat βA3/A1-crystallin gene, termed Nuc1, which has a novel, complex, ocular phenotype. The current study was undertaken to compare the expression pattern of this gene during eye development in wild type and Nuc1 rats by in situ hybridization (ISH) and immunohistochemistry (IHC). βA3/A1-crystallin expression was first detected in the eyes of both wild type and Nuc1 rats at embryonic (E) day 12.5 in the posterior portion of the lens vesicle, and remained limited to the lens fibers throughout fetal life. After birth, βA3/A1-crystallin expression was also detected in the neural retina (specifically in the astrocytes and ganglion cells) and in the retinal pigmented epithelium (RPE). This suggested that βA3/A1-crystallin is not only a structural protein of the lens, but has cellular function(s) in other ocular tissues. In summary, expression of βA3/A1-crystallin is controlled differentially in various eye tissues with lens being the site of greatest expression. Similar staining patterns, detected by ISH and IHC, in wild type and Nuc1 animals suggest that functional differences in the protein, rather than changes in mRNA/protein level of expression, likely account for developmental abnormalities in Nuc1.

摘要

晶体蛋白是晶状体中非常丰富的结构蛋白,也在其他组织中表达。我们之前报道了大鼠βA3/A1-晶体蛋白基因的自发突变,称为 Nuc1,它具有新颖、复杂的眼部表型。本研究旨在通过原位杂交(ISH)和免疫组织化学(IHC)比较野生型和 Nuc1 大鼠眼发育过程中该基因的表达模式。βA3/A1-晶体蛋白的表达首先在野生型和 Nuc1 大鼠的眼部于胚胎(E)第 12.5 天在晶状体泡的后部分被检测到,并且在整个胎儿期仅限于晶状体纤维。出生后,βA3/A1-晶体蛋白的表达也在神经视网膜(特别是星形胶质细胞和神经节细胞)和视网膜色素上皮(RPE)中被检测到。这表明βA3/A1-晶体蛋白不仅是晶状体的结构蛋白,而且在其他眼部组织中具有细胞功能。总之,βA3/A1-晶体蛋白在各种眼部组织中的表达受到差异调控,其中晶状体是表达最丰富的部位。野生型和 Nuc1 动物中通过 ISH 和 IHC 检测到的相似染色模式表明,可能是蛋白质功能的差异而不是 mRNA/蛋白水平表达的变化导致了 Nuc1 中的发育异常。