Evidence map›Paper›PMID 41317192›Full record

ArticleChromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology2025

Development of wheat D genome-specific molecular markers based on subgenome-specific repeats.

Tatiana V Danilova, Ahmed Charif, Katherine Frels, Xiwen Cai

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Article in Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Tatiana V DanilovaUSDA-ARS, Wheat, Sorghum & Forage Research Unit, Lincoln, NE, 68583, USA. tatiana.danilova@usda.gov.
Ahmed CharifDepartment of Agronomy and Horticulture, University of Nebraska, Lincoln, NE, 68583, USA.
Katherine FrelsDepartment of Agronomy and Horticulture, University of Nebraska, Lincoln, NE, 68583, USA.
Xiwen CaiUSDA-ARS, Wheat, Sorghum & Forage Research Unit, Lincoln, NE, 68583, USA. xiwen.cai@usda.gov.

Funding

U.S. Department of Agriculture, Agricultural Research Service 3042-21000-035-000D and 2019-67013-35750
6 · The paper itself

Abstract

Species from the tribe Triticeae can be used for wheat improvement by introgression of valuable genes through wide hybridization. More than 85% of Triticeae genomes consist of repetitive sequences with species-specific content and composition, which can be used to detect introgression chromatin. We developed repeat-based molecular markers specific for the D genome of allopolyploid wheat Triticum aestivum (2n = 6x = 42, AABBDD) and applied them to detect D-genome chromatin in tetraploid wheat T. turgidum (2n = 4x = 28, AABB). To identify wheat subgenome-specific repeats, comparative analysis of low-coverage sequence data was performed using the RepeatExplorer pipeline. Three types of repeats, suitable for the development of D-genome-specific markers were identified: the centromeric retrotransposons Quinta, Afa-family repeats associated with the CACTA DNA transposons and the Ty3/gypsy LTR retrotransposon from the Tekay lineage. Consensus sequences of these repeats were used to select D-genome-specific SNPs and design PCR allelic competitive extension (PACE) assays for detecting D-genome chromatin. The assays were applied to screen introgression populations derived from T. aestivum x T. turgidum crosses. The PACE results were confirmed by fluorescent in situ hybridization, which showed that the markers detected introgressions ranging from translocation segments to intact chromosomes. Given the increasing availability of whole-genome sequence data, the presented approach can be used to develop molecular markers for detection of any introgression regardless of its chromosomal homoeologous group.

Indexed as

Genome, PlantRepetitive Sequences, Nucleic AcidTriticumChromatinChromosomes, PlantGenetic MarkersPolymorphism, Single NucleotideRetroelementsChromatinGenetic MarkersRetroelementsD-subgenomeIntrogression chromatinRepeatsSNP-based markersWheat

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.