Direct interaction of geminin and Six3 in eye development

FD Bene, K Tessmar-Raible, J Wittbrodt - Nature, 2004 - nature.com
Nature, 2004nature.com
Organogenesis in vertebrates requires the tight control of cell proliferation and
differentiation. The homeobox-containing transcription factor Six3 plays a pivotal role, in the
proliferation of retinal precursor cells. In a yeast two-hybrid screen, we identified the DNA
replication-inhibitor geminin as a partner of Six3. Geminin inhibits cell-cycle progression by
sequestering Cdt1 (refs,), the key component for the assembly of the pre-replication
complex. Here, we show that Six3 efficiently competes with Cdt1 directly to bind to geminin …
Abstract
Organogenesis in vertebrates requires the tight control of cell proliferation and differentiation. The homeobox-containing transcription factor Six3 plays a pivotal role, in the proliferation of retinal precursor cells. In a yeast two-hybrid screen, we identified the DNA replication-inhibitor geminin as a partner of Six3. Geminin inhibits cell-cycle progression by sequestering Cdt1 (refs , ), the key component for the assembly of the pre-replication complex. Here, we show that Six3 efficiently competes with Cdt1 directly to bind to geminin, which reveals how Six3 can promote cell proliferation without transcription. In common with Six3 inactivation,, overexpression of the geminin gene (Gem; also known as Gmn) in medaka (Oryzias latipes) induces specific forebrain and eye defects that are rescued by Six3. Conversely, loss of Gem (in common with gain of Six3 (ref. )) promotes retinal precursor-cell proliferation and results in expanded optic vesicles, markedly potentiating Six3 gain-of-function phenotypes. Our data indicate that the transcription factor Six3 and the replication-initiation inhibitor geminin act antagonistically to control the balance between proliferation and differentiation during early vertebrate eye development.
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