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1.
Myocilin基因是与原发性开角型青光眼成因有关的基因。其蛋白产物myocilin蛋白是一种分泌型糖蛋白,具有特征性区域:N端亮氨酸拉链区,中央链接区,C端类嗅质蛋白(嗅素)区。眼组织中,小梁网myocilin蛋白表达水平最高且在细胞内外均可检测到。细胞内myocilin蛋白由小梁网细胞以外泌体样囊泡形式释放至胞外,突变时分泌受阻并异常聚集,使细胞致敏诱发凋亡。细胞外myocilin蛋白通过与一种或多种细胞外基质蛋白相互作用影响细胞的形态、粘接、迁移活动,调节细胞外基质的成分和结构,从而影响房水流出系统。 相似文献
2.
Myocilin is a 55-57-kDa protein that is a member of the olfactomedin protein family. It is expressed in the cornea, sclera and trabecular network of the eye, myelinated peripheral nerves, heart, skeletal muscle, trachea and other tissues. Myocilin binds to a domain of fibronectin, type IV collagen and laminen in the trabecular meshwork of the eye, and its expression is influenced by transforming growth factor beta. Because these extracellular matrix components also are common in the intervertebral disc, the objective of our study was to determine whether the matricellular protein myocilin could be detected in the human or sand rat intervertebral disc using immunohistochemistry and to assess its localization. We investigated 16 specimens of human disc tissue and discs from six sand rats. Three human disc cell cultures grown in three-dimensional culture also were evaluated. Immunocytochemical annulus analysis showed the presence of myocilin within the disc cell cytoplasm in some, but not all, cells. Extracellular matrix in both the human and sand rat disc was negative for myocilin localization. Myocilin is believed to play a role in cell-cell adhesion and/or signaling. Myocilin may have such functions within the disc cell population in a manner similar to tenascin, SPARC and thrombospondin, which are other matricellular proteins recently shown to be present in the disc. 相似文献
3.
Vladimir V. Egorov Natalia A. Grudinina Dmitry V. Lebedev Aram A. Shaldzhyan Alexander V. Slita Alexey K. Sirotkin Andrey V. Vasin Michael M. Shavlovsky 《朊病毒》2013,7(3):248-253
Myocilin is a protein with a molecular weight near 50 kDa. It is expressed in almost all organs and tissues.1 We showed that the peptide DQL ETQ TRE LET AYS NLL RD corresponding to N-terminal Leucine zipper motif (LZM) of the protein is able to form amyloid-like fibrils. The possible role of this motif in myocilin aggregation is discussed. 相似文献
4.
April Crawford Emmanuelle Souzeau Ashish Agar Bronwyn Ridge Andrew Dubowsky Kathryn P. Burdon Jamie E. Craig 《Gene》2014
MYOC gene variants are associated with autosomal dominant primary open angle glaucoma (POAG). In this study, we describe a previously unreported MYOC variant segregating with a POAG phenotype in an Australian family. Two individuals affected with POAG and three unaffected individuals from the same family were recruited through the Australian and New Zealand Registry of Advanced Glaucoma (ANZRAG). Direct sequencing of all MYOC coding exons identified the novel heterozygous single nucleotide transition MYOC:c.1119G>A, p.(Trp373*), predicted to encode an aberrant truncated MYOC protein in two affected siblings. Two unaffected siblings and an unaffected niece were negative for the MYOC sequence variant. 相似文献
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Surgucheva I Park BC Yue BY Tomarev S Surguchov A 《Cellular and molecular neurobiology》2005,25(6):1009-1033
Summary Mutations in the gene encoding human myocilin are associated with some cases of juvenile and early-onset glaucoma. Glaucomatous
mutations prevent myocilin from being secreted. The analysis of the defects associated with mutations point to the existence
of factor(s) in addition to mutations that might be implicated in the development of glaucoma. In the present paper, we found
that interaction of myocilin with one of the members of the synuclein family alters its properties, including its ability
to be secreted. Results of immunoprecipitation show that myocilin is a γ-synuclein-interacting protein. Further analysis demonstrated
that both myocilin and γ-synuclein are expressed in human TM cells, immortalized rat ganglion (RGC-5) cells, and HT22 hippocampal
neurons. According to Western blotting, in addition to monomeric form with molecular weight 17 kDa γ-synuclein is present
as higher molecular weight forms (∼35 and 68 KDa), presumably dimer and tetramer. Myocilin and γ-synuclein have partially
overlapping perinuclear localization. Dexamethasone upregulates myocilin expression in RGC-5 cells and HT22 hippocampal neurons.
We found alterations of myocilin properties as a result of its interaction with γ-synuclein. In cultured cells, γ-synuclein
upregulates myocilin expression, inhibits its secretion and prevents the formation of high molecular weight forms of myocilin.
Although both α-synuclein and γ-synuclein are expressed in HTM cells, only γ-synuclein interacts with myocilin and alters
its properties.
We conclude that myocilin and γ-synuclein interact and as a result, myocilin's properties are changed. Since myocilin and
γ-synuclein have partially overlapping intracellular localization in cell types that are implicated in glaucoma development,
their interaction may play an important role in glaucoma. 相似文献
7.
Athna C. Patterson-Orazem Ahlam N. Qerqez Laura R. Azouz Minh Thu Ma Shannon E. Hill Yemo Ku Lisa A. Schildmeyer Jennifer A. Maynard Raquel L. Lieberman 《The Journal of biological chemistry》2021,297(3)
Recombinant antibodies with well-characterized epitopes and known conformational specificities are critical reagents to support robust interpretation and reproducibility of immunoassays across biomedical research. For myocilin, a protein prone to misfolding that is associated with glaucoma and an emerging player in other human diseases, currently available antibodies are unable to differentiate among the numerous disease-associated protein states. This fundamentally constrains efforts to understand the connection between myocilin structure, function, and disease. To address this concern, we used protein engineering methods to develop new recombinant antibodies that detect the N-terminal leucine zipper structural domain of myocilin and that are cross-reactive for human and mouse myocilin. After harvesting spleens from immunized mice and in vitro library panning, we identified two antibodies, 2A4 and 1G12. 2A4 specifically recognizes a folded epitope while 1G12 recognizes a range of conformations. We matured antibody 2A4 for improved biophysical properties, resulting in variant 2H2. In a human IgG1 format, 2A4, 1G12, and 2H2 immunoprecipitate full-length folded myocilin present in the spent media of human trabecular meshwork (TM) cells, and 2H2 can visualize myocilin in fixed human TM cells using fluorescence microscopy. These new antibodies should find broad application in glaucoma and other research across multiple species platforms. 相似文献
8.
Recent advances in molecular genetics of glaucoma 总被引:2,自引:0,他引:2
Glaucoma represents a heterogeneous group of optic neuropathies, with different genetic bases. It can affect all ages generally with a rise in intra-ocular pressure. Three major types of glaucoma have been reported: primary open angle glaucoma (POAG), primary acute closed angle glaucoma (PACG) and primary congenital glaucoma (PCG), as well as a few others associated with developmental abnormalities. In recent years impressive progress has been made in the molecular genetic studies of POAG and PCG. These include the discovery of three genes – Myocilin, Optineurin and CYP1B1 – defects in which results in Mendelian transmission of glaucoma. Identification of single nucleotide polymorphisms in multiple other genes that are associated with glaucoma and alteration of drug sensitivity are enriching our knowledge regarding the complex nature of the disease. This review attempts to present the recent progress made in the molecular genetics of glaucoma. 相似文献
9.
P. J. Eswari Pandaranayaka J. Kanagavalli S. R. Krishnadas P. Sundaresan S. Krishnaswamy 《World journal of microbiology & biotechnology》2008,24(6):903-907
Human myocilin is a 55 kDa protein that is implicated in primary open angle glaucoma (POAG). Understanding the structure and
folding of the native protein and the mutants that increase aggregation could lead to possible prevention of the condition.
We report here the over expression and purification of the human myocilin in E. coli. The initial expression of recombinant myocilin in E. coli was found to be low. The problem of low yield was found to be due to multiple causes and was overcome using a suitable combination
of vectors, tags, host background and expression protocols. The overexpressed human myocilin was purified by affinity column
chromatography to yield about 8 mg of protein from 1 l of culture. The protein purity and folding were confirmed using electrophoresis,
immunoblotting and fluorescence spectroscopy. Further biophysical characterization and crystallization trials using the recombinant
human myocilin will pave the way for better understanding of the structure–aggregation relationship that is involved in causing
POAG. 相似文献
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