Tubulin tyrosine ligase like 12, a TTLL family member with SET- and TTL-like domains and roles in histone and tubulin modifications and mitosis

• Published in: PloS one 2012-12, Vol.7 (12), p.e51258-e51258
• Main Authors: Brants, Jan, Semenchenko, Kostyantyn, Wasylyk, Christine, Robert, Aude, Carles, Annaick, Zambrano, Alberto, Pradeau-Aubreton, Karine, Birck, Catherine, Schalken, Jack A, Poch, Olivier, de Mey, Jan, Wasylyk, Bohdan
• Format: Article
• Language: English
• Subjects: Amino acids; Binding sites; Biochemistry, Molecular Biology; Biology; Blotting, Western; Catalysis; Cell cycle; Cell division; Cell Line; Cells (Biology); Cellular Biology; Chromosome number; Chromosomes; Electrophoresis, Polyacrylamide Gel; Enzymes; Genomes; Histones - metabolism; Humans; Immunoprecipitation; Life Sciences; Ligases; Medicine; Methylation; Mitosis; Mitosis - physiology; Peptide Synthases - chemistry; Peptide Synthases - metabolism; Peptide Synthases - physiology; Phenols (Class of compounds); Phylogenetics; Phylogeny; Proteins; Trends; Tubulin; Tubulin - metabolism; Tyrosine
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0051258

hTTLL12 is a member of the tubulin tyrosine ligase (TTL) family that is highly conserved in phylogeny. It has both SET-like and TTL-like domains, suggesting that it could have histone methylation and tubulin tyrosine ligase activities. Altered expression of hTTLL12 in human cells leads to specific changes in H4K20 trimethylation, and tubulin detyrosination, hTTLL12 does not catalyse histone methylation or tubulin tyrosination in vitro, as might be expected from the lack of critical amino acids in its SET-like and TTLL-like domains. hTTLL12 misexpression increases mitotic duration and chromosome numbers. These results suggest that hTTLL12 has non-catalytic functions related to tubulin and histone modification, which could be linked to its effects on mitosis and chromosome number stability.