Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway. - Institut Pasteur Access content directly
Journal Articles Journal of Pineal Research Year : 2013

Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway.

Pierre Legrand
Vincent Bondet
Jacques Bellalou
Ahmed Haouz

Abstract

Melatonin is a synchronizer of many physiological processes. Abnormal melatonin signaling is associated with human disorders related to sleep, metabolism, and neurodevelopment. Here, we present the X-ray crystal structure of human N-acetyl serotonin methyltransferase (ASMT), the last enzyme of the melatonin biosynthesis pathway. The polypeptide chain of ASMT consists of a C-terminal domain, which is typical of other SAM-dependent O-methyltransferases, and an N-terminal domain, which intertwines several helices with another monomer to form the physiologically active dimer. Using radioenzymology, we analyzed 20 nonsynonymous variants identified through the 1000 genomes project and in patients with neuropsychiatric disorders. We found that the majority of these mutations reduced or abolished ASMT activity including one relatively frequent polymorphism in the Han Chinese population (N17K, rs17149149). Overall, we estimate that the allelic frequency of ASMT deleterious mutations ranges from 0.66% in Europe to 2.97% in Asia. Mapping of the variants on to the 3-dimensional structure clarifies why some are harmful and provides a structural basis for understanding melatonin deficiency in humans.

Dates and versions

pasteur-01580140 , version 1 (01-09-2017)

Identifiers

Cite

Hany Goubran Botros, Pierre Legrand, Cecile Pagan, Vincent Bondet, Patrick Weber, et al.. Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway.. Journal of Pineal Research, 2013, 54 (1), pp.46-57. ⟨10.1111/j.1600-079X.2012.01020.x⟩. ⟨pasteur-01580140⟩
99 View
0 Download

Altmetric

Share

Gmail Facebook X LinkedIn More