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SWI/SNF亚基INI1包含一个N端带翼螺旋DNA结合结构域,该结构域是神经鞘瘤病中突变的靶点。

The SWI/SNF Subunit INI1 Contains an N-Terminal Winged Helix DNA Binding Domain that Is a Target for Mutations in Schwannomatosis.

作者信息

Allen Mark D, Freund Stefan M V, Zinzalla Giovanna, Bycroft Mark

机构信息

MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0QH, UK.

Centre for Advanced Cancer Therapies, Department of Microbiology, Cell and Tumour Biology and Science for Life Laboratory, Karolinska Institutet, Tomtebodavägen 23, Stockholm 171 65, Sweden.

出版信息

Structure. 2015 Jul 7;23(7):1344-9. doi: 10.1016/j.str.2015.04.021. Epub 2015 Jun 11.

Abstract

SWI/SNF complexes use the energy of ATP hydrolysis to remodel chromatin. In mammals they play a central role in regulating gene expression during differentiation and proliferation. Mutations in SWI/SNF subunits are among the most frequent gene alterations in cancer. The INI1/hSNF5/SMARCB1 subunit is mutated in both malignant rhabdoid tumor, a highly aggressive childhood cancer, and schwannomatosis, a tumor-predisposing syndrome characterized by mostly benign tumors of the CNS. Here, we show that mutations in INI1 that cause schwannomatosis target a hitherto unidentified N-terminal winged helix DNA binding domain that is also present in the BAF45a/PHF10 subunit of the SWI/SNF complex. The domain is structurally related to the SKI/SNO/DAC domain, which is found in a number of metazoan chromatin-associated proteins.

摘要

SWI/SNF复合物利用ATP水解的能量重塑染色质。在哺乳动物中,它们在分化和增殖过程中调节基因表达方面发挥核心作用。SWI/SNF亚基的突变是癌症中最常见的基因改变之一。INI1/hSNF5/SMARCB1亚基在恶性横纹肌样瘤(一种侵袭性很强的儿童癌症)和神经鞘瘤病(一种肿瘤易感综合征,其特征是中枢神经系统大多为良性肿瘤)中均发生突变。在此,我们表明导致神经鞘瘤病的INI1突变靶向一个迄今尚未鉴定的N端带翼螺旋DNA结合结构域,该结构域也存在于SWI/SNF复合物的BAF45a/PHF10亚基中。该结构域在结构上与SKI/SNO/DAC结构域相关,后者存在于许多后生动物染色质相关蛋白中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aec6/4509781/080d33bd1f1a/gr1.jpg

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