Molybdenum cofactor biology, evolution and deficiency

被引:46
|
作者
Mayr, Simon J. [1 ]
Mendel, Ralf-R [2 ]
Schwarz, Guenter [1 ]
机构
[1] Univ Cologne, Ctr Mol Med, Inst Biochem, Dept Chem, Zuelpicher Str 47, D-50674 Cologne, Germany
[2] Braunschweig Univ Technol, Inst Plant Biol, Humboldtstr 1, D-38106 Braunschweig, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2021年 / 1868卷 / 01期
关键词
Alternative splicing; Cysteine catabolism; Inhibitory synapse; Iron-sulfur cluster; Mitochondria; Molybdenum cofactor; MOLYBDOPTERIN SYNTHASE GENE; THALIANA PROVIDES INSIGHT; BICISTRONIC MOCS1 GENE; C-TERMINAL DOMAIN; NIFS-LIKE DOMAIN; CRYSTAL-STRUCTURE; ALDEHYDE OXIDASE; IRON-SULFUR; PROTEIN CONJUGATION; GENOMIC STRUCTURE;
D O I
10.1016/j.bbamcr.2020.118883
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The molybdenum cofactor (Moco) represents an ancient metal-sulfur cofactor, which participates as catalyst in carbon, nitrogen and sulfur cycles, both on individual and global scale. Given the diversity of biological processes dependent on Moco and their evolutionary age, Moco is traced back to the last universal common ancestor (LUCA), while Moco biosynthetic genes underwent significant changes through evolution and acquired additional functions. In this review, focused on eukaryotic Moco biology, we elucidate the benefits of gene fusions on Moco biosynthesis and beyond. While originally the gene fusions were driven by biosynthetic advantages such as coordinated expression of functionally related proteins and product/substrate channeling, they also served as origin for the development of novel functions. Today, Moco biosynthetic genes are involved in a multitude of cellular processes and loss of the according gene products result in severe disorders, both related to Moco biosynthesis and secondary enzyme functions.
引用
收藏
页数:12
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