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鉴定水稻着丝粒和端粒 DNA 结合蛋白。

Identification of centromeric and telomeric DNA-binding proteins in rice.

机构信息

State Key Laboratory for Agrobiotechnology, Institute of Plant Molecular Biology and Agricultural Biotechnology, School of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong.

出版信息

Proteomics. 2013 Mar;13(5):826-32. doi: 10.1002/pmic.201100416. Epub 2013 Jan 31.

Abstract

Centromeres and telomeres are DNA/protein complexes and essential functional components of eukaryotic chromosomes. Previous studies have shown that rice centromeres and telomeres are occupied by CentO (rice centromere satellite DNA) satellite and G-rich telomere repeats, respectively. However, the protein components are not fully understood. DNA-binding proteins associated with centromeric or telomeric DNAs will most likely be important for the understanding of centromere and telomere structure and functions. To capture DNA-specific binding proteins, affinity pull-down technique was applied in this study to isolate rice centromeric and telomeric DNA-binding proteins. Fifty-five proteins were identified for their binding affinity to rice CentO repeat, and 80 proteins were identified for their binding to telomere repeat. One CentO-binding protein, Os02g0288200, was demonstrated to bind to CentO specifically by in vitro assay. A conserved domain, DUF573 with unknown functions was identified in this protein, and proven to be responsible for the specific binding to CentO in vitro. Four proteins identified as telomere DNA-binding proteins in this study were reported by different groups previously. These results demonstrate that DNA affinity pull-down technique is effective in the isolation of sequence-specific binding proteins and will be applicable in future studies of centromere and telomere proteins.

摘要

着丝粒和端粒是 DNA/蛋白质复合物,是真核染色体的必需功能组件。先前的研究表明,水稻着丝粒和端粒分别被 CentO(水稻着丝粒卫星 DNA)卫星和富含 G 的端粒重复序列占据。然而,其蛋白质成分尚未完全阐明。与着丝粒或端粒 DNA 结合的 DNA 结合蛋白很可能对理解着丝粒和端粒的结构和功能至关重要。为了捕获对特定 DNA 具有结合亲和力的蛋白,本研究应用亲和拉下技术来分离水稻着丝粒和端粒 DNA 结合蛋白。有 55 种蛋白因其与水稻 CentO 重复序列的结合亲和力而被鉴定,有 80 种蛋白因其与端粒重复序列的结合亲和力而被鉴定。通过体外实验证明,一种 CentO 结合蛋白 Os02g0288200 能特异性地与 CentO 结合。在该蛋白中鉴定出一个具有未知功能的保守结构域 DUF573,该结构域在体外被证明负责与 CentO 的特异性结合。本研究中鉴定出的 4 种作为端粒 DNA 结合蛋白的蛋白先前曾被不同的研究组报道。这些结果表明,DNA 亲和拉下技术是分离序列特异性结合蛋白的有效方法,将适用于未来对着丝粒和端粒蛋白的研究。

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