TY - JOUR
T1 - Lateral attachment of kinetochores to microtubules is enriched in prometaphase rosette and facilitates chromosome alignment and bi-orientation establishment
AU - Itoh, Go
AU - Ikeda, Masanori
AU - Iemura, Kenji
AU - Amin, Mohammed Abdhullahel
AU - Kuriyama, Sei
AU - Tanaka, Masamitsu
AU - Mizuno, Natsuki
AU - Osakada, Hiroko
AU - Haraguchi, Tokuko
AU - Tanaka, Kozo
N1 - Funding Information:
We thank members of the K.T. laboratory for discussions, and A. Harata for technical assistance. This work was supported by JSPS KAKENHI Grant Numbers JP24370078, JP26640067, JP15H04368, JP16K14604; MEXT KAKENHI Grant Numbers JP24114502, JP26114702; and grants from the Takeda Science Foundation, Princess Takamatsu Cancer Research Fund (10-24210) to K.T., JSPS KAKENHI Grant Number JP26870053 and Cooperative Research Project Program of Joint Usage/Research Center at the Institute of Development, Aging and Cancer, Tohoku University to G.I., JSPS KAKENHI Grant Number JP26870054 to M.I., JSPS KAKENHI Grant Number JP16H06635 to K.I., and MEXT KAKENHI Grant Number JP25116006 to T.H.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Faithful chromosome segregation is ensured by the establishment of bi-orientation; the attachment of sister kinetochores to the end of microtubules extending from opposite spindle poles. In addition, kinetochores can also attach to lateral surfaces of microtubules; called lateral attachment, which plays a role in chromosome capture and transport. However, molecular basis and biological significance of lateral attachment are not fully understood. We have addressed these questions by focusing on the prometaphase rosette, a typical chromosome configuration in early prometaphase. We found that kinetochores form uniform lateral attachments in the prometaphase rosette. Many transient kinetochore components are maximally enriched, in an Aurora B activity-dependent manner, when the prometaphase rosette is formed. We revealed that rosette formation is driven by rapid poleward motion of dynein, but can occur even in its absence, through slow kinetochore movements caused by microtubule depolymerization that is supposedly dependent on kinetochore tethering at microtubule ends by CENP-E. We also found that chromosome connection to microtubules is extensively lost when lateral attachment is perturbed in cells defective in end-on attachment. Our findings demonstrate that lateral attachment is an important intermediate in bi-orientation establishment and chromosome alignment, playing a crucial role in incorporating chromosomes into the nascent spindle.
AB - Faithful chromosome segregation is ensured by the establishment of bi-orientation; the attachment of sister kinetochores to the end of microtubules extending from opposite spindle poles. In addition, kinetochores can also attach to lateral surfaces of microtubules; called lateral attachment, which plays a role in chromosome capture and transport. However, molecular basis and biological significance of lateral attachment are not fully understood. We have addressed these questions by focusing on the prometaphase rosette, a typical chromosome configuration in early prometaphase. We found that kinetochores form uniform lateral attachments in the prometaphase rosette. Many transient kinetochore components are maximally enriched, in an Aurora B activity-dependent manner, when the prometaphase rosette is formed. We revealed that rosette formation is driven by rapid poleward motion of dynein, but can occur even in its absence, through slow kinetochore movements caused by microtubule depolymerization that is supposedly dependent on kinetochore tethering at microtubule ends by CENP-E. We also found that chromosome connection to microtubules is extensively lost when lateral attachment is perturbed in cells defective in end-on attachment. Our findings demonstrate that lateral attachment is an important intermediate in bi-orientation establishment and chromosome alignment, playing a crucial role in incorporating chromosomes into the nascent spindle.
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U2 - 10.1038/s41598-018-22164-5
DO - 10.1038/s41598-018-22164-5
M3 - Article
C2 - 29497093
AN - SCOPUS:85042791913
SN - 2045-2322
VL - 8
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 3888
ER -