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pubmed-article:10717483pubmed:abstractTextPax-6 encodes a transcription factor that is important in the development of eye and CNS. Identification of Pax-6 target genes is crucial for understanding the gene regulatory network in these developmental processes. Using an in-vitro approach of cyclic amplification of the protein binding sequences (CAPBS), we isolated a PAX6 binding sequence from a human single-copy (sc) DNA library. Characterization of this PAX6 binding sequence revealed a 15bp region (hGCalpha1BLs5) that is sufficient for PAX6 specific binding. From a homology search in the GenBank, we found that an hGCalpha1BLs5-like Pax-6 binding site exists in 21 genes (16 from rodent), 15 of which were shown to be able to bind Pax-6 in vitro. Interestingly, some of these sites occur in B1 repetitive elements. Although hGCalpha1BLs5 is highly similar to a region in B1 repetitive elements, PAX6 does not bind to the consensus sequence in B1. However, a single-step mutation in some B1 elements can lead to a gain of function for PAX6 binding. This experimental evidence and phylogenetic analysis raise an interesting speculation for the coevolution between PAX6 regulation and repeat elements. Since a (Pax-6-binding) null B1 element can be re-activated by even a single-step mutation, it has the potential to recruit gene targets for Pax-6 if it is inserted into the regulatory region, and therefore may play a role for evolutionary modification of Pax-6 regulation.lld:pubmed
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pubmed-article:10717483pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:10717483pubmed:articleTitleA novel Pax-6 binding site in rodent B1 repetitive elements: coevolution between developmental regulation and repeated elements?lld:pubmed
pubmed-article:10717483pubmed:affiliationDepartment of Biochemistry, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA. sa51001@odin.mdacc.tmc.edulld:pubmed
pubmed-article:10717483pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10717483pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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