Histone methyltransferase and histone methylation in inflammatory T-cell responses

Author:

He Shan1,Tong Qing12,Bishop Dennis Keith3,Zhang Yi4

Affiliation:

1. Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109-5942, USA

2. International Joint Cancer Institute, The Second Military Medical University, Shanghai, China

3. Department of Surgery, University of Michigan, Ann Arbor, MI, USA

4. Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109-5942, USA.

Abstract

During immune responses, T cells require tightly controlled expression of transcriptional programs to regulate the balance between beneficial and harmful immunity. These transcriptional programs are critical for the lineage specification of effector T cells, the production of effector cytokines and molecules, and the development and maintenance of memory T cells. An emerging theme is that post-translational modification of histones by methylation plays an important role in orchestrating the expression of transcriptional programs in T cells. In this article, we provide a broad overview of histone methylation signatures for effector molecules and transcription factors in T cells, and the functional importance of histone methyltransferases in regulating T-cell immune responses.

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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