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東大医科学研究所

東京大学医科学研究所学友会セミナーをご案内します。

日時 7月27日 木曜日 午後3時から4時
場所 東京大学医科学研究所合同ラボ棟2階セミナー室
(地下鉄南北線白金台駅下車
建物が傾斜地にたっているため病院側から見ると
1階にあたるところが2階です。ご注意下さい。
迷った方は5449-5664にお電話下さい。)

William H. Klein&s_comma; PhD
Professor and Chairman Robert A. Welch Distinguished Chair in Chemistry Department of Biochemistry and Molecular Biology&s_comma; Unit 1000 The University of Texas M. D. Anderson Cancer Center

演題:"A gene regulatory network for retinal ganglion cell development"

Research Synopsis Differentiated cell types originate during development from precursor cells that generally have the potential to give rise to multiple cell types.
Choosing an individual cell fate relies on both the precursor cell’s external environment and its internal genetic program at a particular moment in time. My laboratory is investigating how gene expression programs are regulated when precursor cells differentiate into individual cell types. We are especially interested in the role of cell-type specific transcription factors and their ability to alter programs of gene expression. We use diverse models to delineate how particular transcription factors work to program cellular differentiation.
In one project using mice&s_comma; we have identified some of the key transcription factors that regulate the differentiation of the ganglion cells of the neural retina. Retinal ganglion cells are responsible for transmitting electrical impulses from the retina to the primary visual centers of the brain via the optic nerve. Although retinal ganglion cells are essential for vision&s_comma; how they form and why they die in retinal disease is poorly understood. We have discovered that two transcription factors play
critical roles in the formation of retinal ganglion cells. A factor called Math5 is required for making precursor cells competent to advance to a retinal ganglion cell fate while a second factor called Brn3b is necessary for overt retinal ganglion cell differentiation. We have placed Math5 and Brn3b as central nodes in a genetic regulatory network responsible for retinal ganglion cell formation. Our current investigations are aimed at elaborating the network using a combination of genetic and genomic approaches.

References
Mu X&s_comma; et al. and Klein WH (2004). Discrete gene sets depend on POU domain transcription factor Brn3b/Brn-3.2/POU4f2 for their expression in the mouse embryonic retina. Development 131:1197-1210.

Mu X&s_comma; Klein WH (2004). A gene regulatory hierarchy for retinal ganglion cell specification and differentiation. Semin Cell Dev Biol 15:115-123.

Mu X&s_comma; et al&s_comma; and Klein WH (2005). Ganglion cells are required for normal progenitor cell proliferation but not cell-fate determination or patterning in the developing mouse retina. Curr Biol 15:525-530.

Mu X&s_comma; et al&s_comma; and Klein WH (2005). A gene network downstream of transcription factor Math5 regulates retinal progenitor cell competence and ganglion cell fate. Dev Biol 289:467-481.



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