Dissecting the maize genome by using chromosome addition and radiation hybrid lines

  1. Ralf G. Kynast*,
  2. Ron J. Okagaki*,
  3. Mark W. Galatowitsch*,
  4. Shannon R. Granath*,
  5. Morrison S. Jacobs*,
  6. Adrian O. Stec*,
  7. Howard W. Rines*,, and
  8. Ronald L. Phillips*,
  1. *Department of Agronomy and Plant Genetics and Center for Microbial and Plant Genomics, University of Minnesota, 1991 Upper Buford Circle, St. Paul, MN 55108; and Plant Science Research Unit, Department of Agriculture-Agricultural Research Service, St. Paul, MN 55108
  1. Contributed by Ronald L. Phillips, May 13, 2004

Abstract

We have developed from crosses of oat (Avena sativa L.) and maize (Zea mays L.) 50 fertile lines that are disomic additions of individual maize chromosomes 1-9 and chromosome 10 as a short-arm telosome. The whole chromosome 10 addition is available only in haploid oat background. Most of the maize chromosome disomic addition lines have regular transmission; however, chromosome 5 showed diminished paternal transmission, and chromosome 10 is transmitted to offspring only as a short-arm telosome. To further dissect the maize genome, we irradiated monosomic additions with γ rays and recovered radiation hybrid (RH) lines providing low- to medium-resolution mapping for most of the maize chromosomes. For maize chromosome 1, mapping 45 simple-sequence repeat markers delineated 10 groups of RH plants reflecting different chromosome breaks. The present chromosome 1 RH panel dissects this chromosome into eight physical segments defined by the 10 groups of RH lines. Genomic in situ hybridization revealed the physical size of a distal region, which is represented by six of the eight physical segments, as being ≈20% of the length of the short arm, representing ≈one-third of the genetic chromosome 1 map. The distal ≈20% of the physical length of the long arm of maize chromosome 1 is represented by a single group of RH lines that spans >23% of the total genetic map. These oat-maize RH lines provide valuable tools for physical mapping of the complex highly duplicated maize genome and for unique studies of inter-specific gene interactions.

Footnotes

  • To whom correspondence should be addressed. E-mail: phill005{at}umn.edu.

  • This report was presented at the International Congress “In the Wake of the Double Helix: From the Green Revolution to the Gene Revolution,” held May 27-31, 2003, at the University of Bologna, Bologna, Italy. The scientific organizers were Roberto Tuberosa, University of Bologna, Bologna, Italy; Ronald L. Phillips, University of Minnesota, St. Paul, MN; and Mike Gale, John Innes Center, Norwich, United Kingdom. The Congress web site (www.doublehelix.too.it) reports the list of sponsors and the abstracts.

  • Abbreviations: BC, backcross; GISH, genomic in situ hybridization; RH, radiation hybrid; SSR marker, simple-sequence repeat marker.

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