» Articles » PMID: 16517762

Arabidopsis TEBICHI, with Helicase and DNA Polymerase Domains, is Required for Regulated Cell Division and Differentiation in Meristems

Overview
Journal Plant Cell
Specialties Biology
Cell Biology
Date 2006 Mar 7
PMID 16517762
Citations 58
Authors
Affiliations
Soon will be listed here.
Abstract

In plant meristems, each cell divides and differentiates in a spatially and temporally regulated manner, and continuous organogenesis occurs using cells derived from the meristem. We report the identification of the Arabidopsis thaliana TEBICHI (TEB) gene, which is required for regulated cell division and differentiation in meristems. The teb mutants show morphological defects, such as short roots, serrated leaves, and fasciation, as well as defective patterns of cell division and differentiation in the meristem. The TEB gene encodes a homolog of Drosophila MUS308 and mammalian DNA polymerase theta, which prevent spontaneous or DNA damage-induced production of DNA double strand breaks. As expected from the function of animal homologs, teb mutants show constitutively activated DNA damage responses. Unlike other fasciation mutants with activated DNA damage responses, however, teb mutants do not activate transcriptionally silenced genes. teb shows an accumulation of cells expressing cyclinB1;1:GUS in meristems, suggesting that constitutively activated DNA damage responses in teb lead to a defect in G2/M cell cycle progression. Furthermore, other fasciation mutants, such as fasciata2 and tonsoku/mgoun3/brushy1, also show an accumulation of cells expressing cyclinB1;1:GUS in meristems. These results suggest that cell cycle progression at G2/M is important for the regulation of the pattern of cell division and of differentiation during plant development.

Citing Articles

A non-tethering role for the Drosophila linker domain in promoting damage resolution.

Blanch J, Krishnamurthy M, McVey M bioRxiv. 2024; .

PMID: 39253446 PMC: 11383001. DOI: 10.1101/2024.08.27.609911.


Inhibitors against DNA Polymerase I Family of Enzymes: Novel Targets and Opportunities.

Kannan S, Gillespie S, Picking W, Picking W, Lorson C, Singh K Biology (Basel). 2024; 13(4).

PMID: 38666816 PMC: 11048162. DOI: 10.3390/biology13040204.


How to use CRISPR/Cas9 in plants: from target site selection to DNA repair.

Pribylova A, Fischer L J Exp Bot. 2024; 75(17):5325-5343.

PMID: 38648173 PMC: 11389839. DOI: 10.1093/jxb/erae147.


Genetic dissection of mutagenic repair and T-DNA capture at CRISPR-induced DNA breaks in .

Kamoen L, Kralemann L, van Schendel R, van Tol N, Hooykaas P, de Pater S PNAS Nexus. 2024; 3(3):pgae094.

PMID: 38463035 PMC: 10923293. DOI: 10.1093/pnasnexus/pgae094.


Transformation and regeneration of DNA polymerase Θ mutant rice plants.

Nishizawa-Yokoi A, Gelvin S Plant Direct. 2023; 7(9):e526.

PMID: 37681196 PMC: 10480422. DOI: 10.1002/pld3.526.


References
1.
Shima N, Hartford S, Duffy T, Wilson L, Schimenti K, Schimenti J . Phenotype-based identification of mouse chromosome instability mutants. Genetics. 2003; 163(3):1031-40. PMC: 1462482. DOI: 10.1093/genetics/163.3.1031. View

2.
Zhang Z, Shibahara K, Stillman B . PCNA connects DNA replication to epigenetic inheritance in yeast. Nature. 2000; 408(6809):221-5. DOI: 10.1038/35041601. View

3.
Suzuki T, Inagaki S, Nakajima S, Akashi T, Ohto M, Kobayashi M . A novel Arabidopsis gene TONSOKU is required for proper cell arrangement in root and shoot apical meristems. Plant J. 2004; 38(4):673-84. DOI: 10.1111/j.1365-313X.2004.02074.x. View

4.
Garcia V, Bruchet H, Camescasse D, Granier F, Bouchez D, Tissier A . AtATM is essential for meiosis and the somatic response to DNA damage in plants. Plant Cell. 2003; 15(1):119-32. PMC: 143473. DOI: 10.1105/tpc.006577. View

5.
Abraham R . Cell cycle checkpoint signaling through the ATM and ATR kinases. Genes Dev. 2001; 15(17):2177-96. DOI: 10.1101/gad.914401. View