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Review
. 2024 Dec;120(6):2356-2366.
doi: 10.1111/tpj.17142. Epub 2024 Nov 15.

Synthetic minichromosomes in plants: past, present, and promise

Affiliations
Review

Synthetic minichromosomes in plants: past, present, and promise

James A Birchler et al. Plant J. 2024 Dec.

Abstract

The status of engineered mini-chromosomes/artificial chromosomes/synthetic chromosomes in plants is summarized. Their promise is that they provide a means to accumulate foreign genes on an independent entity other than the normal chromosomes, which would facilitate stacking of novel traits in a way that would not be linked to endogenous genes and that would facilitate transfer between lines. Centromeres in plants are epigenetic, and therefore the isolation of DNA underlying centromeres and reintroduction into plant cells will not establish a functional kinetochore, which obviates this approach for in vitro assembly of plant artificial chromosomes. This issue was bypassed by using telomere-mediated chromosomal truncation to produce mini-chromosomes with little more than an endogenous centromere that could in turn be used as a foundation to build synthetic chromosomes. Site-specific recombinases and various iterations of CRISPR-Cas9 editing provide many tools for the development and re-engineering of synthetic chromosomes.

Keywords: B chromosomes; CRISPR‐Cas9; artificial chromosomes; engineered minichromosomes; gene editing; genetic engineering; haploids; site‐specific recombinases; synthetic chromosomes.

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REFERENCES

    1. Ahkong, Q.F., Howell, J.I., Lucy, J.A., Safwat, F., Davey, M.R. & Cocking, E.C. (1975) Fusion of hen erythrocytes with yeast protoplast induced by polyethylene glycol. Nature, 255, 66–67.
    1. Akbudak, M.A. & Srivastava, V. (2011) Improved FLP recombinase, FLPe, efficiently removes marker gene transgene locus developed by Cre‐lox mediated site‐specific gene integration in rice. Molecular Biotechnology, 49, 82–89.
    1. Albert, H., Dale, E.C., Lee, E. & Ow, D.W. (1995) Site‐specific integration of DNA into wild‐type and mutant lox sites placed in the plant genome. The Plant Journal, 7, 649–659.
    1. Anand, A., Wu, E., Li, Z., TeRonde, S., Arling, M., Lenders, B. et al. (2019) High efficiency Agrobacterium‐mediated site‐specific gene integration in maize utilizing the FLP‐FRT recombination system. Plant Biotechnology Journal, 17, 1636–1645.
    1. Banaei‐Moghaddam, A.M., Schubert, V., Kumke, K., Weiss, O., Klemme, S., Nagaki, K. et al. (2012) Nondisjunction in favor of a chromosome: the mechanism of rye B chromosome drive during pollen mitosis. Plant Cell, 24, 4124–4134.

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