TY - JOUR
T1 - Linking cytoplasmic dynein and transport of Rab8 vesicles to the midbody during cytokinesis by the doublecortin domain-containing 5 protein
AU - Kaplan, Anna
AU - Reiner, Orly
N1 - Israel Science Foundation [270/04, 47/10, 1062/08]; Israel Cancer Association [20090073]; Minerva Foundation; Federal German Ministry for Education and Research; Benoziyo Center for Neurological Diseases; Helen and Martin Kimmel Stem Cell Research Institute; David and Fela Shapell Family Center for Genetic Disorders ResearchThis research was supported by the Israel Science Foundation [grant numbers 270/04, 47/10 to O.R.]; the Legacy Heritage Biomedical Program of the Israel Science Foundation [grant number 1062/08 to O.R.]; the Israel Cancer Association [grant number 20090073 to O.R.]; the Minerva Foundation with funding from the Federal German Ministry for Education and Research; the Benoziyo Center for Neurological Diseases; the Helen and Martin Kimmel Stem Cell Research Institute; and the David and Fela Shapell Family Center for Genetic Disorders Research. O.R. is an incumbent of the Berstein-Mason Professorial Chair of Neurochemistry.
PY - 2011/12
Y1 - 2011/12
N2 - Completion of mitosis requires microtubule-dependent transport of membranes to the midbody. Here, we identified a role in cytokinesis for doublecortin domain-containing protein 5 (DCDC5), a member of the doublecortin protein superfamily. DCDC5 is a microtubuleassociated protein expressed in both specific and dynamic fashions during mitosis. We show that DCDC5 interacts with cytoplasmic dynein and Rab8 (also known as Ras-related protein Rab-8A), as well as with the Rab8 nucleotide exchange factor Rabin8 (also known as Rab-3A-interacting protein). Following DCDC5 knockdown, the durations of the metaphase to anaphase transition and cytokinesis, and the proportion of multinucleated cells increases, whereas cell viability decreases. Furthermore, knockdown of DCDC5 or addition of a dynein inhibitor impairs the entry of Golgi-complex-derived Rab8-positive vesicles to the midbody. These findings suggest that DCDC5 plays an important role in mediating dynein-dependent transport of Rab8-positive vesicles and in coordinating late cytokinesis.
AB - Completion of mitosis requires microtubule-dependent transport of membranes to the midbody. Here, we identified a role in cytokinesis for doublecortin domain-containing protein 5 (DCDC5), a member of the doublecortin protein superfamily. DCDC5 is a microtubuleassociated protein expressed in both specific and dynamic fashions during mitosis. We show that DCDC5 interacts with cytoplasmic dynein and Rab8 (also known as Ras-related protein Rab-8A), as well as with the Rab8 nucleotide exchange factor Rabin8 (also known as Rab-3A-interacting protein). Following DCDC5 knockdown, the durations of the metaphase to anaphase transition and cytokinesis, and the proportion of multinucleated cells increases, whereas cell viability decreases. Furthermore, knockdown of DCDC5 or addition of a dynein inhibitor impairs the entry of Golgi-complex-derived Rab8-positive vesicles to the midbody. These findings suggest that DCDC5 plays an important role in mediating dynein-dependent transport of Rab8-positive vesicles and in coordinating late cytokinesis.
UR - http://www.scopus.com/inward/record.url?scp=84856850675&partnerID=8YFLogxK
U2 - https://doi.org/10.1242/jcs.085407
DO - https://doi.org/10.1242/jcs.085407
M3 - مقالة
SN - 0021-9533
VL - 124
SP - 3989
EP - 4000
JO - Journal of Cell Science
JF - Journal of Cell Science
IS - 23
ER -