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Published on: June 25, 2013
The mismatch repair protein MSH6 regulates somatic recombination in Arabidopsis thaliana
Valentina Gonzalez1, Claudia P Spampinato1
1Centro de Estudios Fotosintéticos y Bioquímicos (CEFOBI), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, 2000, Rosario, Argentina.
Abstract:
The mismatch repair (MMR) pathway promotes genome stability by controlling the fidelity of replication and recombination. The first step of the pathway involves recognition of the mismatch by heterodimers composed of MutS homologs (MSH). Although MSH6 has been well characterized in yeasts and humans, the role of the plant protein has not been extensively studied. We first analyzed gene expression in Arabidopsis thaliana. The use of transgenic plants expressing the β-glucuronidase (GUS) reporter gene under the control of approximately 1-kb region upstream of the start codon of the AtMSH6 gene demonstrated that MSH6 is preferentially expressed in undifferentiated cells with an intense cell division rate. We then examined protein function in meiotic and somatic recombination. Suppression of AtMSH6 did not affect the rate of meiotic recombination, but increased the frequency of recombination between two homeologous repeats of a marker gene by 3-fold relative to wild-type plants. Expression of the AtMSH6 gene under the control of its own promoter in msh6 homozygous mutant plants rescued the altered somatic recombination phenotype. We conclude that MSH6 shows a functional conservation across different biological kingdoms and a functional specificity in plants.
Insights
The plant protein MSH6 is crucial for genome stability, particularly in somatic recombination, showing conserved function across species. Its expression is highest in rapidly dividing cells, highlighting its role in DNA repair.
Area of Science:
- Molecular Biology
- Genetics
- Plant Science
Background:
- The mismatch repair (MMR) pathway is essential for maintaining genome stability by correcting errors during DNA replication and recombination.
- MutS homologs (MSH) initiate the MMR pathway by recognizing DNA mismatches.
- While MSH6 is well-studied in yeast and humans, its function in plants remains less understood.
Purpose of the Study:
- To investigate the gene expression patterns of Arabidopsis thaliana MSH6 (AtMSH6).
- To elucidate the functional role of AtMSH6 in meiotic and somatic recombination processes in plants.
Main Methods:
- Analysis of AtMSH6 gene expression using transgenic Arabidopsis plants with a β-glucuronidase (GUS) reporter gene.
- Assessment of AtMSH6 function by examining meiotic and somatic recombination rates in wild-type and msh6 mutant plants.
- Complementation of the msh6 mutant phenotype by expressing AtMSH6 under its native promoter.
Main Results:
- AtMSH6 is predominantly expressed in undifferentiated plant cells with high division rates.
- Suppression of AtMSH6 did not impact meiotic recombination but significantly increased somatic recombination frequency (3-fold) between homeologous repeats.
- Restoring AtMSH6 expression in mutant plants rescued the elevated somatic recombination phenotype.
Conclusions:
- AtMSH6 plays a critical role in suppressing somatic recombination in plants, indicating functional specificity.
- The study confirms functional conservation of MSH6 across different biological kingdoms.
- AtMSH6 is important for maintaining genome stability, particularly in the context of somatic DNA repair in plants.
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