Leiz Janna, Rutkiewicz Maria, Birchmeier Carmen, Heinemann Udo, Schmidt-Ott Kai M
Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Nephrology and Intensive Care Medicine, Hindenburgdamm 30, 12203 Berlin, Germany.
Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association (MDC), Molecular and Translational Kidney Research, Robert-Rössle-Str. 10, 13125 Berlin, Germany.
Med Genet. 2021 Aug 14;33(2):147-155. doi: 10.1515/medgen-2021-2073. eCollection 2021 Jun.
Transcription factors (TFs) bind DNA in a sequence-specific manner and thereby regulate target gene expression. TF binding and its regulatory activity is highly context dependent, and is not only determined by specific cell types or differentiation stages but also relies on other regulatory mechanisms, such as DNA and chromatin modifications. Interactions between TFs and their DNA binding sites are critical mediators of phenotypic variation and play important roles in the onset of disease. A continuously growing number of studies therefore attempts to elucidate TF:DNA interactions to gain knowledge about regulatory mechanisms and disease-causing variants. Here we summarize how TF-binding characteristics and the impact of variants can be investigated, how bioinformatic tools can be used to analyze and predict TF:DNA binding, and what additional information can be obtained from the TF protein structure.
转录因子(TFs)以序列特异性方式结合DNA,从而调节靶基因表达。TF结合及其调节活性高度依赖于上下文,不仅由特定细胞类型或分化阶段决定,还依赖于其他调节机制,如DNA和染色质修饰。TF与其DNA结合位点之间的相互作用是表型变异的关键介质,在疾病发生中起重要作用。因此,越来越多的研究试图阐明TF:DNA相互作用,以了解调节机制和致病变体。在这里,我们总结了如何研究TF结合特征和变体的影响,如何使用生物信息学工具分析和预测TF:DNA结合,以及从TF蛋白质结构中可以获得哪些额外信息。