<?xml version="1.0" encoding="UTF-8"?><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcq="http://purl.org/dc/terms/"><records count="1" morepages="false" start="1" end="1"><record rownumber="1"><dc:product_type>Journal Article</dc:product_type><dc:title>Synthetic maize centromeres transmit chromosomes across generations</dc:title><dc:creator>Dawe, R. Kelly; Gent, Jonathan I.; Zeng, Yibing; Zhang, Han; Fu, Fang-Fang; Swentowsky, Kyle W.; Kim, Dong Won; Wang, Na; Liu, Jianing; Piri, Rebecca D.</dc:creator><dc:corporate_author/><dc:editor/><dc:description>Centromeres are long, often repetitive regions of genomes that bind
kinetochore proteins and ensure normal chromosome segregation.
Engineering centromeres that function in vivo has proven to be difficult.
Here we describe a tethering approach that activates functional maize
centromeres at synthetic sequence arrays. A LexA-CENH3 fusion protein
was used to recruit native Centromeric Histone H3 (CENH3) to long arrays of
LexO repeats on a chromosome arm. Newly recruited CENH3 was sufficient
to organize functional kinetochores that caused chromosome breakage,
releasing chromosome fragments that were passed through meiosis and
into progeny. Several fragments formed independent neochromosomes
with centromeres localized over the LexO repeat arrays. The new
centromeres were self-sustaining and transmitted neochromosomes to
subsequent generations in the absence of the LexA-CENH3 activator.
Our results demonstrate the feasibility of using synthetic centromeres
for karyotype engineering applications.</dc:description><dc:publisher>Nature Plants</dc:publisher><dc:date>2023-03-01</dc:date><dc:nsf_par_id>10494278</dc:nsf_par_id><dc:journal_name>Nature Plants</dc:journal_name><dc:journal_volume>9</dc:journal_volume><dc:journal_issue>3</dc:journal_issue><dc:page_range_or_elocation>433 to 441</dc:page_range_or_elocation><dc:issn>2055-0278</dc:issn><dc:isbn/><dc:doi>https://doi.org/10.1038/s41477-023-01370-8</dc:doi><dcq:identifierAwardId>2040218</dcq:identifierAwardId><dc:subject/><dc:version_number/><dc:location/><dc:rights/><dc:institution/><dc:sponsoring_org>National Science Foundation</dc:sponsoring_org></record></records></rdf:RDF>