- THIS ARTICLE
- Full Text
- Full Text (PDF)
- Data Supplement
- Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Email this article to a friend
- Related articles in Genetics
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Lough, A. N.
- Articles by Newton, K. J.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Lough, A. N.
- Articles by Newton, K. J.
Genetics, Vol. 178, 47-55, January 2008, Copyright © 2008
doi:10.1534/genetics.107.079624
Mitochondrial DNA Transfer to the Nucleus Generates Extensive Insertion Site Variation in Maize
Ashley N. Lough*,1,
Leah M. Roark*,1,
Akio Kato
,
Thomas S. Ream
,
Jonathan C. Lamb
,
James A. Birchler* and
Kathleen J. Newton*,2
* Division of Biological Sciences, University of Missouri, Columbia, Missouri 65211,
Faculty of Agriculture, Kyoto Prefectural University, Sakyo-ku, Kyoto-shi, Kyoto-fu, 606-0823, Japan,
Biology Department, Washington University, St. Louis, Missouri 63130 and
Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas 77843
2 Corresponding author: Division of Biological Sciences, 324 Tucker Hall, University of Missouri, Columbia, MO 65211-7400.
E-mail: newtonk{at}missouri.edu
Mitochondrial DNA (mtDNA) insertions into nuclear chromosomes have been documented in a number of eukaryotes. We used fluorescence in situ hybridization (FISH) to examine the variation of mtDNA insertions in maize. Twenty overlapping cosmids, representing the 570-kb maize mitochondrial genome, were individually labeled and hybridized to root tip metaphase chromosomes from the B73 inbred line. A minimum of 15 mtDNA insertion sites on nine chromosomes were detectable using this method. One site near the centromere on chromosome arm 9L was identified by a majority of the cosmids. To examine variation in nuclear mitochondrial DNA sequences (NUMTs), a mixture of labeled cosmids was applied to chromosome spreads of ten diverse inbred lines: A188, A632, B37, B73, BMS, KYS, Mo17, Oh43, W22, and W23. The number of detectable NUMTs varied dramatically among the lines. None of the tested inbred lines other than B73 showed the strong hybridization signal on 9L, suggesting that there is a recent mtDNA insertion at this site in B73. Different sources of B73 and W23 were examined for NUMT variation within inbred lines. Differences were detectable, suggesting either that mtDNA is being incorporated or lost from the maize nuclear genome continuously. The results indicate that mtDNA insertions represent a major source of nuclear chromosomal variation.
Related articles in Genetics:
ISSUE HIGHLIGHTS
Genetics 2008 178: NP.