Journal
DEVELOPMENTAL CELL
Volume 42, Issue 2, Pages 181-+Publisher
CELL PRESS
DOI: 10.1016/j.devcel.2017.06.019
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Funding
- JSPS KAKENHI [25221106, 16H06279, 15H05972, 17H06167, 17K07501, 26440190, 25116002, 25250023, 16H01304]
- Grants-in-Aid for Scientific Research [15H05970, 17K15043, 16H01304, 16H06279, 17H06167, 26440190, 16K18491, 16J10043, 25116002, 17K07501, 15K21761, 15H05972] Funding Source: KAKEN
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Centromeres are specified and maintained by sequence-independent epigenetic mechanisms through the incorporation of CENP-A into centromeres. Given that CENP-A incorporation requires the Mis18 complex to be in the centromere region, it is necessary to precisely understand how the Mis18 complex localizes to the centromere region. Here, we showed that centromere localization of the Mis18 complex depends on CENP-A, but not CENP-C or CENP-T, in chicken DT40 cells. Furthermore, we demonstrated that M18BP1/KNL2, a member of the Mis18 complex, contained the CENP-C-like motif in chicken and other vertebrates, which is essential for centromere localization and M18BP1/KNL2 function in DT40 cells. We also showed that in vitro reconstituted CENP-A nucleosome, but not H3 nucleosome, bound to the CENP-C-like motif containing M18BP1/KNL2. Based on these results, we conclude thatM18BP1/KNL2 is essential for centromere formation through direct binding to CENP-A nucleosome in non-mammalian vertebrates. This explains how new CENP-A recognizes the centromere position.
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