The tubulin code and its role in controlling microtubule properties and functions

被引:562
作者
Janke, Carsten [1 ,2 ]
Magiera, Maria M. [1 ,2 ]
机构
[1] PSL Res Univ, Inst Curie, CNRS UMR3348, Orsay, France
[2] Univ Paris Saclay, CNRS UMR3348, Orsay, France
关键词
III BETA-TUBULIN; ALPHA-TUBULIN; POSTTRANSLATIONAL MODIFICATION; TYROSINE-LIGASE; DYNAMIC INSTABILITY; MONOCLONAL-ANTIBODY; BRAIN TUBULIN; MOUSE-BRAIN; IN-VITRO; TYROSYLTUBULIN LIGASE;
D O I
10.1038/s41580-020-0214-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mechanical and dynamic properties of microtubules are determined by their complement of subunits, known as tubulin isotypes, and the post-translational modifications found on these isotypes. This concept is known as the 'tubulin code'. The regulation of microtubules and microtubule-associated proteins by this code is critical for the correct function of a range of tissues. Consequently, recent studies have linked perturbation of the tubulin code to disease, including neurodegenerative diseases. Microtubules are core components of the eukaryotic cytoskeleton with essential roles in cell division, shaping, motility and intracellular transport. Despite their functional heterogeneity, microtubules have a highly conserved structure made from almost identical molecular building blocks: the tubulin proteins. Alternative tubulin isotypes and a variety of post-translational modifications control the properties and functions of the microtubule cytoskeleton, a concept known as the 'tubulin code'. Here we review the current understanding of the molecular components of the tubulin code and how they impact microtubule properties and functions. We discuss how tubulin isotypes and post-translational modifications control microtubule behaviour at the molecular level and how this translates into physiological functions at the cellular and organism levels. We then go on to show how fine-tuning of microtubule function by some tubulin modifications can affect homeostasis and how perturbation of this fine-tuning can lead to a range of dysfunctions, many of which are linked to human disease.
引用
收藏
页码:307 / 326
页数:20
相关论文
共 319 条
[1]   Centrioles resist forces applied on centrosomes during G2/M transition [J].
Abal, M ;
Keryer, G ;
Bornens, M .
BIOLOGY OF THE CELL, 2005, 97 (06) :425-434
[2]   The combination of whole-exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophies [J].
Abu Diab, Alaa ;
AlTalbishi, Ala'a ;
Rosin, Boris ;
Kanaan, Moien ;
Kamal, Lara ;
Swaroop, Anand ;
Chowers, Itay ;
Banin, Eyal ;
Sharon, Dror ;
Khateb, Samer .
ACTA OPHTHALMOLOGICA, 2019, 97 (06) :E877-E886
[3]   Crystal structure of the tubulin tyrosine carboxypeptidase complex VASH1-SVBP [J].
Adamopoulos, Athanassios ;
Landskron, Lisa ;
Heidebrecht, Tatjana ;
Tsakou, Foteini ;
Bleijerveld, Onno B. ;
Altelaar, Maarten ;
Nieuwenhuis, Joppe ;
Celie, Patrick H. N. ;
Brummelkamp, Thijn R. ;
Perrakis, Anastassis .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2019, 26 (07) :567-+
[4]   Mitotic phosphorylation by NEK6 and NEK7 reduces the microtubule affinity of EML4 to promote chromosome congression [J].
Adib, Rozita ;
Montgomery, Jessica M. ;
Atherton, Joseph ;
O'Regan, Laura ;
Richards, Mark W. ;
Straatman, Kees R. ;
Roth, Daniel ;
Straube, Anne ;
Bayliss, Richard ;
Moores, Carolyn A. ;
Fry, Andrew M. .
SCIENCE SIGNALING, 2019, 12 (594)
[5]   TUBULIN EVOLUTION - CILIATE-SPECIFIC EPITOPES ARE CONSERVED IN THE CILIARY TUBULIN OF METAZOA [J].
ADOUTTE, A ;
CLAISSE, M ;
MAUNOURY, R ;
BEISSON, J .
JOURNAL OF MOLECULAR EVOLUTION, 1985, 22 (03) :220-229
[6]  
AHMAD FJ, 1993, J NEUROSCI, V13, P856
[7]   Vasohibins/SVBP are tubulin carboxypeptidases (TCPs) that regulate neuron differentiation [J].
Aillaud, Chrystelle ;
Bosc, Christophe ;
Peris, Leticia ;
Bosson, Anouk ;
Heemeryck, Pierre ;
Van Dijk, Juliette ;
Le Friec, Julien ;
Boulan, Benoit ;
Vossier, Frederique ;
Sanman, Laura E. ;
Syed, Salahuddin ;
Amara, Neri ;
Coute, Yohann ;
Lafanechere, Laurence ;
Denarier, Eric ;
Delphin, Christian ;
Pelletier, Laurent ;
Humbert, Sandrine ;
Bogyo, Matthew ;
Andrieux, Annie ;
Rogowski, Krzysztof ;
Moutin, Marie-Jo .
SCIENCE, 2017, 358 (6369) :1448-1452
[8]   Evidence for new C-terminally truncated variants of α- and β-tubulins [J].
Aillaud, Chrystelle ;
Bosc, Christophe ;
Saoudi, Yasmina ;
Denarier, Eric ;
Peris, Leticia ;
Sago, Laila ;
Taulet, Nicolas ;
Cieren, Adeline ;
Tort, Olivia ;
Magiera, Maria M. ;
Janke, Carsten ;
Redeker, Virginie ;
Andrieux, Annie ;
Moutin, Marie-Jo .
MOLECULAR BIOLOGY OF THE CELL, 2016, 27 (04) :640-653
[9]   MEC-17 is an α-tubulin acetyltransferase [J].
Akella, Jyothi S. ;
Wloga, Dorota ;
Kim, Jihyun ;
Starostina, Natalia G. ;
Lyons-Abbott, Sally ;
Morrissette, Naomi S. ;
Dougan, Scott T. ;
Kipreos, Edward T. ;
Gaertig, Jacek .
NATURE, 2010, 467 (7312) :218-U111
[10]   Spindle asymmetry drives non-Mendelian chromosome segregation [J].
Akera, Takashi ;
Chmatal, Lukas ;
Trimm, Emily ;
Yang, Karren ;
Aonbangkhen, Chanat ;
Chenoweth, David M. ;
Janke, Carsten ;
Schultz, Richard M. ;
Lampson, Michael A. .
SCIENCE, 2017, 358 (6363) :668-+