TY - JOUR
T1 - Molecular architecture of the kinetochore-microtubule attachment site is conserved between point and regional centromeres
AU - Joglekar, Ajit P.
AU - Bouck, David
AU - Finley, Ken
AU - Liu, Xingkun
AU - Wan, Yakun
AU - Berman, Judith
AU - He, Xiangwei
AU - Salmon, E. D.
AU - Bloom, Kerry S.
PY - 2008/5/19
Y1 - 2008/5/19
N2 - Point and regional centromeres specify a unique site on each chromosome for kinetochore assembly. The point centromere in budding yeast is a unique 150-bp DNA sequence, which supports a kinetochore with only one microtubule attachment. In contrast, regional centromeres are complex in architecture, can be up to 5 Mb in length, and typically support many kinetochore-microtubule attachments. We used quantitative fluorescence microscopy to count the number of core structural kinetochore protein complexes at the regional centromeres in fission yeast and Candida albicans. We find that the number of CENP-A nucleosomes at these centromeres reflects the number of kinetochore-microtubule attachments instead of their length. The numbers of kinetochore protein complexes per microtubule attachment are nearly identical to the numbers in a budding yeast kinetochore. These findings reveal that kinetochores with multiple microtubule attachments are mainly built by repeating a conserved structural subunit that is equivalent to a single microtubule attachment site.
AB - Point and regional centromeres specify a unique site on each chromosome for kinetochore assembly. The point centromere in budding yeast is a unique 150-bp DNA sequence, which supports a kinetochore with only one microtubule attachment. In contrast, regional centromeres are complex in architecture, can be up to 5 Mb in length, and typically support many kinetochore-microtubule attachments. We used quantitative fluorescence microscopy to count the number of core structural kinetochore protein complexes at the regional centromeres in fission yeast and Candida albicans. We find that the number of CENP-A nucleosomes at these centromeres reflects the number of kinetochore-microtubule attachments instead of their length. The numbers of kinetochore protein complexes per microtubule attachment are nearly identical to the numbers in a budding yeast kinetochore. These findings reveal that kinetochores with multiple microtubule attachments are mainly built by repeating a conserved structural subunit that is equivalent to a single microtubule attachment site.
UR - http://www.scopus.com/inward/record.url?scp=44149083326&partnerID=8YFLogxK
U2 - 10.1083/jcb.200803027
DO - 10.1083/jcb.200803027
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C2 - 18474626
AN - SCOPUS:44149083326
VL - 181
SP - 587
EP - 594
JO - Journal of Cell Biology
JF - Journal of Cell Biology
SN - 0021-9525
IS - 4
ER -