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Since then CBP has been shown to bind to &amp;gt;100 additional proteins and functions in a multitude of different developmental contexts. Among other activities, CBP is known to influence development by remodeling chromatin, by serving as a transcriptional coactivator, and by interacting with terminal members of several signaling transduction cascades. Reductions in CBP activity are the underlying cause of Rubinstein-Taybi syndrome, which is, in part, characterized by several eye defects, including strabismus, cataracts, juvenile glaucoma, and coloboma of the eyelid, iris, and lens. Development of the Drosophila melanogaster compound eye is also inhibited in flies that are mutant for CBP. However, the vast array of putative protein interactions and the wide-ranging roles played by CBP within a single tissue such as the retina can often complicate the analysis of CBP loss-of-function mutants. Through a series of genetic screens we have identified several genes that could either serve as downstream transcriptional targets or encode for potential CBP-binding partners and whose association with eye development has hitherto been unknown. The identification of these new components may provide new insight into the roles that CBP plays in retinal development. Of particular interest is the identification that the CREB transcription factor appears to function with CBP at multiple stages of retinal development.<\/jats:p>","DOI":"10.1534\/genetics.105.045450","type":"journal-article","created":{"date-parts":[[2005,7,6]],"date-time":"2005-07-06T03:23:20Z","timestamp":1120620200000},"page":"1655-1672","source":"Crossref","is-referenced-by-count":20,"title":["A Genetic Screen Identifies Putative Targets and Binding Partners of CREB-Binding Protein in the Developing Drosophila Eye"],"prefix":"10.1093","volume":"171","author":[{"given":"Jason","family":"Anderson","sequence":"first","affiliation":[{"name":"Department of Biology, Indiana University, Bloomington, Indiana 47401"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rohan","family":"Bhandari","sequence":"additional","affiliation":[{"name":"Department of Biology, Indiana University, Bloomington, Indiana 47401"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Justin P","family":"Kumar","sequence":"additional","affiliation":[{"name":"Department of Biology, Indiana University, Bloomington, Indiana 47401"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2005,12,1]]},"reference":[{"key":"2022010801144735100_BIB1","doi-asserted-by":"crossref","first-page":"334","DOI":"10.1007\/s004120000092","volume":"109","year":"2000","journal-title":"Chromosoma"},{"key":"2022010801144735100_BIB2","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1101\/SQB.1985.050.01.025","volume":"50","year":"1985","journal-title":"Cold Spring Harbor Symp. 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