The role of myocilin/TIGR in glaucoma: Results of the Glaucoma Research Foundation Catalyst Meeting in Berkeley, California, March 2000

Citation
Er. Tamm et P. Russell, The role of myocilin/TIGR in glaucoma: Results of the Glaucoma Research Foundation Catalyst Meeting in Berkeley, California, March 2000, J GLAUCOMA, 10(4), 2001, pp. 329-339
Citations number
105
Categorie Soggetti
Optalmology
Journal title
JOURNAL OF GLAUCOMA
ISSN journal
10570829 → ACNP
Volume
10
Issue
4
Year of publication
2001
Pages
329 - 339
Database
ISI
SICI code
1057-0829(200108)10:4<329:TROMIG>2.0.ZU;2-S
Abstract
Approximately 3 years ago, the first major (biochemical, molecular biologic , and biologic) insight into primary open-angle glaucoma was the finding th at mutations in the myocilin (MYOC/TIGR) gene were related to certain forms of juvenile onset of this disease. Since then, a great deal of work has be en done to determine the possible mechanisms by which MYOC/TIGR might cause not only juvenile but also adult-onset primary open-angle glaucoma. To ass ess the current knowledge and those areas in which more research is necessa ry, a meeting of scientists was held by the Glaucoma Research Foundation of San Francisco, California in the spring of 2000. This meeting attempted to concentrate on the MYOC/TIGR protein rather than the genetics of this gene . Possible functions and roles of this protein intracellularly and extracel lularly were critically examined and discussed. Normal transcriptional and translational events and the effect of mutations on these events were explo red. The discussions yielded insight not only in those areas in which impor tant information is known but also in vital areas in which little is curren tly understood. This review attempts to summarize the current knowledge reg arding MYOC/TIGR and to elucidate the points that the people attending the meeting thought needed further study.