» Articles » PMID: 9362502

Neocentromere-mediated Chromosome Movement in Maize

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 1997 Dec 31
PMID 9362502
Citations 60
Authors
Affiliations
Soon will be listed here.
Abstract

Neocentromere activity is a classic example of nonkinetochore chromosome movement. In maize, neocentromeres are induced by a gene or genes on Abnormal chromosome 10 (Ab10) which causes heterochromatic knobs to move poleward at meiotic anaphase. Here we describe experiments that test how neocentromere activity affects the function of linked centromere/kinetochores (kinetochores) and whether neocentromeres and kinetochores are mobilized on the spindle by the same mechanism. Using a newly developed system for observing meiotic chromosome congression and segregation in living maize cells, we show that neocentromeres are active from prometaphase through anaphase. During mid-anaphase, normal chromosomes move on the spindle at an average rate of 0.79 micron/min. The presence of Ab10 does not affect the rate of normal chromosome movement but propels neocentromeres poleward at rates as high as 1.4 micron/min. Kinetochore-mediated chromosome movement is only marginally affected by the activity of a linked neocentromere. Combined in situ hybridization/immunocytochemistry is used to demonstrate that unlike kinetochores, neocentromeres associate laterally with microtubules and that neocentromere movement is correlated with knob size. These data suggest that microtubule depolymerization is not required for neocentromere motility. We argue that neocentromeres are mobilized on microtubules by the activity of minus end-directed motor proteins that interact either directly or indirectly with knob DNA sequences.

Citing Articles

Mechanisms, Machinery, and Dynamics of Chromosome Segregation in .

Duffy M, Ngaw M, Polsky S, Marzec A, Zhang S, Dzierzgowski O Genes (Basel). 2025; 15(12.

PMID: 39766873 PMC: 11675298. DOI: 10.3390/genes15121606.


Remarkable chromosomes and karyotypes: A top 10 list.

Sullivan W Mol Biol Cell. 2024; 35(4):pe1.

PMID: 38517328 PMC: 11064663. DOI: 10.1091/mbc.E23-12-0498.


A kinesin-based approach for inducing chromosome-specific mis-segregation in human cells.

Truong M, Cane-Gasull P, de Vries S, Nijenhuis W, Wardenaar R, Kapitein L EMBO J. 2023; 42(10):e111559.

PMID: 37038978 PMC: 10183822. DOI: 10.15252/embj.2022111559.


Synthetic maize centromeres transmit chromosomes across generations.

Dawe R, Gent J, Zeng Y, Zhang H, Fu F, Swentowsky K Nat Plants. 2023; 9(3):433-441.

PMID: 36928774 DOI: 10.1038/s41477-023-01370-8.


Non-B-form DNA tends to form in centromeric regions and has undergone changes in polyploid oat subgenomes.

Liu Q, Yi C, Zhang Z, Su H, Liu C, Huang Y Proc Natl Acad Sci U S A. 2022; 120(1):e2211683120.

PMID: 36574697 PMC: 9910436. DOI: 10.1073/pnas.2211683120.


References
1.
Dawe R, Cande W . Induction of centromeric activity in maize by suppressor of meiotic drive 1. Proc Natl Acad Sci U S A. 1996; 93(16):8512-7. PMC: 38703. DOI: 10.1073/pnas.93.16.8512. View

2.
Tokai N, Toyoshima Y, Yonemura S, Tsukita S, Inoue J, Yamamota T . Kid, a novel kinesin-like DNA binding protein, is localized to chromosomes and the mitotic spindle. EMBO J. 1996; 15(3):457-67. PMC: 449964. View

3.
Wordeman L, Mitchison T . Identification and partial characterization of mitotic centromere-associated kinesin, a kinesin-related protein that associates with centromeres during mitosis. J Cell Biol. 1995; 128(1-2):95-104. PMC: 2120339. DOI: 10.1083/jcb.128.1.95. View

4.
Pfarr C, Coue M, Grissom P, Hays T, Porter M, McIntosh J . Cytoplasmic dynein is localized to kinetochores during mitosis. Nature. 1990; 345(6272):263-5. DOI: 10.1038/345263a0. View

5.
Afshar K, Barton N, Hawley R, Goldstein L . DNA binding and meiotic chromosomal localization of the Drosophila nod kinesin-like protein. Cell. 1995; 81(1):129-38. DOI: 10.1016/0092-8674(95)90377-1. View