The α-and β-tubulin folding pathways
SA Lewis, G Tian, NJ Cowan - Trends in cell biology, 1997 - cell.com
The α—β tubulin heterodimer is the subunit from which microtubules are assembled. The
pathway leading to correctly folded α-and β-tubulins is unusually complex: it involves cycles …
pathway leading to correctly folded α-and β-tubulins is unusually complex: it involves cycles …
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
K Poirier, N Lebrun, L Broix, G Tian, Y Saillour… - Nature …, 2013 - nature.com
The genetic causes of malformations of cortical development (MCD) remain largely
unknown. Here we report the discovery of multiple pathogenic missense mutations in …
unknown. Here we report the discovery of multiple pathogenic missense mutations in …
[HTML][HTML] Mutations in α-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans
The development of the mammalian brain is dependent on extensive neuronal migration.
Mutations in mice and humans that affect neuronal migration result in abnormal lamination …
Mutations in mice and humans that affect neuronal migration result in abnormal lamination …
Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria
XH Jaglin, K Poirier, Y Saillour, E Buhler, G Tian… - Nature …, 2009 - nature.com
Polymicrogyria is a relatively common but poorly understood defect of cortical development
characterized by numerous small gyri and a thick disorganized cortical plate lacking normal …
characterized by numerous small gyri and a thick disorganized cortical plate lacking normal …
[HTML][HTML] Pathway leading to correctly folded β-tubulin
G Tian, Y Huang, H Rommelaere, J Vandekerckhove… - Cell, 1996 - cell.com
We describe the complete β-tubulin folding pathway. Folding intermediates produced via
ATP–dependent interaction with cytosolic chaperonin undergo a sequence of interactions …
ATP–dependent interaction with cytosolic chaperonin undergo a sequence of interactions …
[HTML][HTML] Mutations in TUBB8 and Human Oocyte Meiotic Arrest
R Feng, Q Sang, Y Kuang, X Sun, Z Yan… - … England Journal of …, 2016 - Mass Medical Soc
Background Human reproduction depends on the fusion of a mature oocyte with a sperm
cell to form a fertilized egg. The genetic events that lead to the arrest of human oocyte …
cell to form a fertilized egg. The genetic events that lead to the arrest of human oocyte …
Tubulin subunits exist in an activated conformational state generated and maintained by protein cofactors
G Tian, SA Lewis, B Feierbach, T Stearns… - The Journal of cell …, 1997 - rupress.org
The production of native α/β tubulin heterodimer in vitro depends on the action of cytosolic
chaperonin and several protein cofactors. We previously showed that four such cofactors …
chaperonin and several protein cofactors. We previously showed that four such cofactors …
[PDF][PDF] Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities
The formation of the mammalian cortex requires the generation, migration, and
differentiation of neurons. The vital role that the microtubule cytoskeleton plays in these …
differentiation of neurons. The vital role that the microtubule cytoskeleton plays in these …
[PDF][PDF] Chaperonin-mediated folding of actin and tubulin.
SA Lewis, G Tian, IE Vainberg… - The Journal of cell …, 1996 - europepmc.org
HE central dogma of molecular biology holds that proteins contain within their primary amino
acid sequence all the information that is required to dictate their three-dimensional structure …
acid sequence all the information that is required to dictate their three-dimensional structure …
Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos
R Feng, Z Yan, B Li, M Yu, Q Sang, G Tian… - Journal of medical …, 2016 - jmg.bmj.com
Background TUBB8 is a primate-specific β-tubulin isotype whose expression is confined to
oocytes and the early embryo. We previously found that mutations in TUBB8 caused oocyte …
oocytes and the early embryo. We previously found that mutations in TUBB8 caused oocyte …