Microtubule-Associated Serine/Threonine (MAST) Kinases in Development and Disease

Author:

Rumpf Marie1ORCID,Pautz Sabine2,Drebes Benedikt1,Herberg Friedrich W.2ORCID,Müller Hans-Arno J.1ORCID

Affiliation:

1. Department of Developmental Genetics, Institute of Biology, University of Kassel, 34321 Kassel, Germany

2. Department of Biochemistry, Institute of Biology, University of Kassel, 34321 Kassel, Germany

Abstract

Microtubule-Associated Serine/Threonine (MAST) kinases represent an evolutionary conserved branch of the AGC protein kinase superfamily in the kinome. Since the discovery of the founding member, MAST2, in 1993, three additional family members have been identified in mammals and found to be broadly expressed across various tissues, including the brain, heart, lung, liver, intestine and kidney. The study of MAST kinases is highly relevant for unraveling the molecular basis of a wide range of different human diseases, including breast and liver cancer, myeloma, inflammatory bowel disease, cystic fibrosis and various neuronal disorders. Despite several reports on potential substrates and binding partners of MAST kinases, the molecular mechanisms that would explain their involvement in human diseases remain rather obscure. This review will summarize data on the structure, biochemistry and cell and molecular biology of MAST kinases in the context of biomedical research as well as organismal model systems in order to provide a current profile of this field.

Funder

University of Kassel

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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