First published online April 1, 2005; 10.1105/tpc.104.030643
The Plant Cell 17:1412-1423 (2005)
© 2005 American Society of Plant Biologists
Molecular and Functional Dissection of the Maize B Chromosome Centromere
Weiwei Jina,
Jonathan C. Lambb,
Juan M. Vegab,
R. Kelly Dawec,
James A. Birchlerb,1 and
Jiming Jianga,1
a Department of Horticulture, University of Wisconsin–Madison, Madison, Wisconsin 53706
b Division of Biological Science, University of Missouri, Columbia, Missouri 65211
c Department of Plant Biology, University of Georgia, Athens, Georgia 30602
1 To whom correspondence should be addressed. E-mail birchlerj{at}missouri.edu or jjiang1{at}wisc.edu; fax 573-882-0123 or 608-262-4743.
The centromere of the maize (Zea mays) B chromosome contains several megabases of a B-specific repeat (ZmBs), a 156-bp satellite repeat (CentC), and centromere-specific retrotransposons (CRM elements). Here, we demonstrate that only a small fraction of the ZmBs repeats interacts with CENH3, the histone H3 variant specific to centromeres. CentC, which marks the CENH3-associated chromatin in maize A centromeres, is restricted to an  700-kb domain within the larger context of the ZmBs repeats. The breakpoints of five B centromere misdivision derivatives are mapped within this domain. In addition, the fraction of this domain remaining after misdivision correlates well with the quantity of CENH3 on the centromere. Thus, the functional boundaries of the B centromere are mapped to a relatively small CentC- and CRM-rich region that is embedded within multimegabase arrays of the ZmBs repeat. Our results demonstrate that the amount of CENH3 at the B centromere can be varied, but with decreasing amounts, the function of the centromere becomes impaired.
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