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ZENODO
Dataset . 2026
License: CC BY
Data sources: Datacite
ZENODO
Dataset . 2026
License: CC BY
Data sources: Datacite
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DNA sequences of PCR fragments obtained from genomic DNA of Solanum tuberosum cv. Désirée mutants in GI.04 and GI.12 genes

Authors: Bánfalvi, Zsófia;

DNA sequences of PCR fragments obtained from genomic DNA of Solanum tuberosum cv. Désirée mutants in GI.04 and GI.12 genes

Abstract

Species Cultivar Mutated gene Mutant line Allele name Solanum tuberosum Désirée GI.04 eGI.04/1 eGI.04/1a eGI.04/1b eGI.04/1c eGI.04/1d eGI.04/2 eGI.04/2a and 2b eGI.04/2c and 2d eGI.04/3 eGI.04/3a eGI.04/3b eGI.04/3c eGI.04/3d eGI,04/3e eGI.04/3f eGI.04/3g eGI.04/3h mGI.04/1 mGI.04/1a mGI.04/1b mGI.04/1c mGI.04/1d mGI.04/2 mGI.04/2a mGI.04/2b mGI.04/2c mGI.04/2d mGI.04/3 mGI.04/3a mGI.04/3b mGI.04/3c mGI.04/3d GI.12 eGI.12/1 eGI.12/1a and 1b eGI.12/1c and 1d eGI.12/2 eGI.12/2a eGI.12/2b eGI.12/2c eGI.12/2d eGI.12/3 eGI.12/3a eGI.12/3b eGI.12/3c eGI.12/3d mGI.12/1 mGI.12/1a mGI.12/1b mGI.12/1c mGI.12/1d mGI.12/2 mGI.12/2a mGI.12/2b mGI.12/2c mGI.12/2d mGI.12/3 mGI.12/3a mGI.12/3b mGI.12/3c mGI.12/3d GI.04 mGI.412/1 mGI.412/1a mGI.412/1b mGI.412/1c mGI.412/1d mGI.412/2 mGI.412/2a mGI.412/2b mGI.412/2c mGI.412/2d mGI.412/3 mGI.412/3a mGI.412/3b mGI.412/3c mGI.412/3d GI.12 mGI.412/1 mGI.412/1a mGI.412/1b mGI.412/1c mGI.412/1d mGI.412/2 mGI.412/2a mGI.412/2b mGI.412/2c and 2d mGI.412/3 mGI.412/3a mGI.412/3b mGI.412/3c and 3d

Earliness of tuberisation is an important agronomic trait. It was demonstrated earlier that GIGANTEA (GI), a plant-specific nuclear protein that regulates multiple processes, is indirectly involved in tuberisation in a diploid potato. Commercial potatoes, including the cultivar Désirée, are tetraploids and carry two copies of GI genes, designated GI.04 and GI.12. The aim of our study was to explore the role of the two GI genes in Désirée in relation to tuberisation. To obtain information on GI.04 and GI.12 functions in Désirée, mutations were introduced into the two genes individually and simultaneously using the CRISPR/Cas9 system. Two different segments of the genes were targeted by gRNAs. PCR was used for mutant identification. Three mutants from each mutagenesis were selected, and the mutations were localised by generating PCR fragments using primers surrounding the targeted regions and sequencing them. Sequences of the PCR fragments are available from the uploaded file.

Keywords

CRISPR/Cas9, Mutation mapping, Plant development, Solanum tuberosum, tuberization

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
Average
Average