Isolation and characterization of SATB2, a novel AT-rich DNA binding protein expressed in development- and cell-specific manner in the rat brain

被引:77
作者
Szemes, M
Gyorgy, A
Paweletz, C
Dobi, A
Agoston, DV
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Anat Physiol & Genet, Bethesda, MD 20814 USA
[2] Univ Bristol, Sch Med Sci, Dept Pharmacol, Bristol BS1 8TD, Avon, England
[3] Merck Res Labs, Dept Mol Profiling Proteom, Rahway, NJ 07065 USA
[4] USUHS, Dept Surg, Ctr Prostate Dis Res, Rockville, MD 20852 USA
[5] Uniformed Serv Univ Hlth Sci, Program Neurosci, Bethesda, MD 20814 USA
关键词
DNA affinity; mass spectrometry; MAR; SAR; chromatin; structure; neuronal; differentiation;
D O I
10.1007/s11064-005-9012-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
AT-rich DNA elements play an important role in regulating cell-specific gene expression. One of the AT-rich DNA binding proteins, SATB1 is a novel type of transcription factor that regulates gene expression in the hematopoietic lineage through chromatin modification. Using DNA-affinity purification followed by mass spectrometry we identified and isolated a related protein, SATB2 from the developing rat cerebral cortex. SATB2 shows homology to SATB1 and the rat protein is practically identical to the mouse and human SATB2. Using competitive EMSA, we show that recombinant SATB2 protein binds with high affinity and specificity to AT-rich dsDNA. Using RT-PCR, Western analysis and immunohistochemistry we demonstrate that SATB2 expression is restricted to a subset of postmitotic, differentiating neurons in the rat neocortex at ages E16 and P4. We suggest that similar to its homologue SATB1, SATB2 is also involved in regulating gene expression through altering chromatin structure in differentiating cortical neurons.
引用
收藏
页码:237 / 246
页数:10
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