z-logo
open-access-imgOpen Access
Genome-Wide Distribution of TransposedDissociationElements in Maize
Author(s) -
Erik Vollbrecht,
Jon Duvick,
Justin P. Schares,
Kevin R. Ahern,
Prasit Deewatthanawong,
Ling Xu,
Liza Conrad,
Kazuhiro Kikuchi,
Tammy A. Kubinec,
Bradford D. Hall,
Rebecca Weeks,
Erica UngerWallace,
Michael G. Muszynski,
Volker Brendel,
Thomas P. Brutnell
Publication year - 2010
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.109.073452
Subject(s) - biology , genome , dissociation (chemistry) , zea mays , genetics , distribution (mathematics) , computational biology , evolutionary biology , agronomy , gene , mathematical analysis , chemistry , mathematics
The maize (Zea mays) transposable element Dissociation (Ds) was mobilized for large-scale genome mutagenesis and to study its endogenous biology. Starting from a single donor locus on chromosome 10, over 1500 elements were distributed throughout the genome and positioned on the maize physical map. Genetic strategies to enrich for both local and unlinked insertions were used to distribute Ds insertions. Global, regional, and local insertion site trends were examined. We show that Ds transposed to both linked and unlinked sites and displayed a nonuniform distribution on the genetic map around the donor r1-sc:m3 locus. Comparison of Ds and Mutator insertions reveals distinct target preferences, which provide functional complementarity of the two elements for gene tagging in maize. In particular, Ds displays a stronger preference for insertions within exons and introns, whereas Mutator insertions are more enriched in promoters and 5'-untranslated regions. Ds has no strong target site consensus sequence, but we identified properties of the DNA molecule inherent to its local structure that may influence Ds target site selection. We discuss the utility of Ds for forward and reverse genetics in maize and provide evidence that genes within a 2- to 3-centimorgan region flanking Ds insertions will serve as optimal targets for regional mutagenesis.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom