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

C Janke, MM Magiera - Nature Reviews Molecular Cell Biology, 2020 - nature.com
Microtubules are core components of the eukaryotic cytoskeleton with essential roles in cell
division, shaping, motility and intracellular transport. Despite their functional heterogeneity …

The tubulin code, from molecules to health and disease

ED McKenna, SL Sarbanes… - Annual Review of …, 2023 - annualreviews.org
Microtubules are essential dynamic polymers composed of α/β-tubulin heterodimers. They
support intracellular trafficking, cell division, cellular motility, and other essential cellular …

Ciliopathies

DA Braun, F Hildebrandt - Cold Spring Harbor …, 2017 - cshperspectives.cshlp.org
Nephronophthisis-related ciliopathies (NPHP-RC) are a group of inherited diseases that
affect genes encoding proteins that localize to primary cilia or centrosomes. With few …

The cilium: cellular antenna and central processing unit

JJ Malicki, CA Johnson - Trends in cell biology, 2017 - cell.com
Cilia mediate an astonishing diversity of processes. Recent advances provide unexpected
insights into the regulatory mechanisms of cilium formation, and reveal diverse regulatory …

A near-infrared fluorophore for live-cell super-resolution microscopy of cellular proteins

G Lukinavičius, K Umezawa, N Olivier, A Honigmann… - Nature …, 2013 - nature.com
The ideal fluorescent probe for bioimaging is bright, absorbs at long wavelengths and can
be implemented flexibly in living cells and in vivo. However, the design of synthetic …

Septins: the fourth component of the cytoskeleton

S Mostowy, P Cossart - Nature reviews Molecular cell biology, 2012 - nature.com
Septins belong to a family of proteins that is highly conserved in eukaryotes and is
increasingly recognized as a novel component of the cytoskeleton. All septins are GTP …

Genotype–phenotype correlates in Joubert syndrome: A review

S Gana, V Serpieri, EM Valente - American Journal of Medical …, 2022 - Wiley Online Library
Joubert syndrome (JS) is a genetically heterogeneous primary ciliopathy characterized by a
pathognomonic cerebellar and brainstem malformation, the “molar tooth sign,” and variable …

Tubulin polyglutamylation differentially regulates microtubule‐interacting proteins

M Genova, L Grycova, V Puttrich, MM Magiera… - The EMBO …, 2023 - embopress.org
Tubulin posttranslational modifications have been predicted to control cytoskeletal functions
by coordinating the molecular interactions between microtubules and their associating …

Graded control of microtubule severing by tubulin glutamylation

ML Valenstein, A Roll-Mecak - Cell, 2016 - cell.com
Microtubule-severing enzymes are critical for the biogenesis and maintenance of complex
microtubule arrays in axons, spindles, and cilia where tubulin detyrosination, acetylation …

Joubert syndrome: congenital cerebellar ataxia with the molar tooth

M Romani, A Micalizzi, EM Valente - The Lancet Neurology, 2013 - thelancet.com
Joubert syndrome is a congenital cerebellar ataxia with autosomal recessive or X-linked
inheritance, the diagnostic hallmark of which is a unique cerebellar and brainstem …