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Updated: Aug 9, 2026

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Measuring Endoreduplication by Flow Cytometry of Isolated Tuber Protoplasts
Published on: March 9, 2018
A pseudoduplication in Lycopersicon pimpinellifolium
C M Rick1, S D Tanksley, J F Fobes
1Department of Vegetable Crops, University of California, Davis, California 95616.
Summary
Genetic analysis revealed that a double-banded peroxidase variant (Prx-2) in Lycopersicon pimpinellifolium is not due to gene duplication. An independent gene modifies the Prx-2 product, creating multiple bands.
Area of Science:
- Plant genetics
- Molecular biology
- Biochemistry
Background:
- A previous survey identified a double-banded variant of Prx-2 in Lycopersicon pimpinellifolium.
- This variant exhibited anomalous segregation patterns inconsistent with a single-locus model.
Purpose of the Study:
- To genetically analyze the cause of the double-banded Prx-2 variant.
- To determine if the variant results from gene duplication or modification by another gene.
Main Methods:
- Genetic crosses were performed between the double-banded Prx-2 variant and various Prx-2 alleles.
- Simultaneous segregation analysis was conducted with alleles of the tightly linked Prx-3 gene.
- Electrophoretic analysis was used to separate and identify peroxidase isozymes.
Main Results:
- Segregation data did not support a single locus model for the double-banded variant.
- The double-banded phenotype segregated independently of the Prx-3 gene, ruling out linkage and duplication at the Prx-2 locus.
- Evidence suggests an independent gene, mPx2(1), modifies the Prx-2 gene product post-translationally.
Conclusions:
- Multiple banding in peroxidases does not necessarily indicate gene duplication.
- Post-translational modification by an independent gene is a plausible explanation for the observed variant.
- Careful genetic analysis is crucial to avoid misinterpreting banding patterns as evidence of gene duplication.
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