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. 1999 Jan 28;18(4):1041-51.
doi: 10.1038/sj.onc.1202406.

Involvement of poly (ADP-ribose)-polymerase in the Pax-6 gene regulation in neuroretina

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VSports最新版本 - Involvement of poly (ADP-ribose)-polymerase in the Pax-6 gene regulation in neuroretina

S Plaza et al. Oncogene. .

Abstract

The quail Pax-6 gene is expressed from two promoters named P0 and P1. P0 promoter is under the control of a neuroretina-specific enhancer (EP). This enhancer activates the P0 promoter specifically in neuroretina cells and in a developmental stage-dependent manner. The EP enhancer binds efficiently, as revealed by southwestern experiments, to a 110 kDa protein present in neuroretina cells but not in Quail Embryos Cells and Retinal Pigmented Epithelium which do not express the P0-initiated mRNAs. To study the role of p110 in Pax-6 regulation, we have purified the p110 from neuroretina cells extracts. Based on the peptide sequence of the purified protein, we have identified the p110 as the poly(ADP-ribose) polymerase (PARP). Using bandshift experiments and footprinting studies, we present evidence that PARP is a component of protein complexes bound to the EP enhancer that increases the on rate of the protein complex formation to DNA. Using PARP inhibitors (3AB and 6. 5 Hphe), we show that these products are able to inhibit EP enhancer activity in neuroretina cells VSports手机版. Finally, we demonstrate that these inhibitors are able to decrease the expression of the P0-initiated mRNA in the MC29-infected RPE cells which, in contrast to the RPE cells, accumulated the PARP in response to v-myc expression. Our results suggest that PARP is involved in the Pax-6 regulation. .

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