Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2009 Apr;118(2):157-77.
doi: 10.1007/s00412-008-0191-3. Epub 2008 Nov 18.

Artificial chromosome formation in maize (Zea mays L.)

Affiliations

Artificial chromosome formation in maize (Zea mays L.)

Evgueni V Ananiev et al. Chromosoma. 2009 Apr.

Abstract

We report on the construction of maize minichromosomes using shuttle vectors harboring native centromeric segments, origins of replication, selectable marker genes, and telomeric repeats. These vectors were introduced into scutellar cells of maize immature embryos by microprojectile bombardment. Several independent transformation events were identified containing minichromosomes in addition to the normal diploid complement of 20 maize chromosomes. Immunostaining indicated that the minichromosomes recruited centromeric protein C, which is a specific component of the centromere/kinetochore complex. Minichromosomes were estimated to be 15-30 Mb in size based on cytological measurements. Fluorescent in situ hybridization (FISH) showed that minichromosomes contain the centromeric, telomeric, and exogenous unique marker sequences interspersed with maize retrotransposons. Minichromosomes were detected for at least a year in actively dividing callus cultures, providing evidence for their stability through numerous cell cycles. Plants were regenerated and minichromosomes were detected in root tips, providing confirmation of their normal replication and transmission during mitosis and through organogenesis. Assembly of maize artificial chromosomes may provide a tool to study centromere function and a foundation for developing new high capacity vectors for plant functional genomics and breeding.

PubMed Disclaimer

References

    1. Nucleic Acids Res. 2005 Jan 26;33(2):587-96 - PubMed
    1. Plant Cell. 2004 Mar;16(3):571-81 - PubMed
    1. Genetics. 2003 Oct;165(2):809-19 - PubMed
    1. Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11042-6 - PubMed
    1. Biochem Biophys Res Commun. 2004 Aug 20;321(2):280-90 - PubMed