Maize chromatin introgression’s effect in oat × maize addition lines

The addition lines derived from oat (Avena sativa L.) × maize (Zea mays L.) crosses constitute a unique tool for studying gene expression and the structure of chromatin, as well as a source of agronomically desirable traits in the context of new intergeneric hybrid cultivars. Therefore, for a better understanding of the introgression of maize chromatin into the oat genome, a comprehensive analysis of oat × maize lines was conducted. The presence of maize chromatin was confirmed in three tested lines by PCR-based amplification of the maize retrotransposon Grande-1, and verified by genomic in situ hybridization. Interestingly, the addition lines containing cytologically-detectable maize chromosomes showed a possible disturbance of the Rabl-like centromere-telomere polarization typical for oat. Moreover, the maize chromatin was consistently positioned near the nuclear periphery. The maize chromatin introgression caused a prolonged DNA replication phase, altering cell cycle dynamics, and may led to mitotic abnormalities, such as the formation of micronuclei and anaphase chromosome bridges. The introgression lines also showed morphological and physiological changes: smaller seeds, hampered seedlings' growth, and reduced yield parameters (number of flowers/seeds per plant/panicle and seed weight). These findings shed more light on the consequences of the maize chromatin introgression into the oat genome and the stability and utility of the obtained hybrids.

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Publication Details

Journal
Journal of Applied Genetics
Published
2026-06-18
DOI
https://doi.org/10.1007/s13353-026-01086-3
Primary Topic
Chromosomal and Genetic Variations
Type
article
Field-Weighted Citation Impact
0.00

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article

Maize chromatin introgression’s effect in oat × maize addition lines

Edyta Skrzypek, Mahmoud Said, Marzena Warchoł, Tomasz Warzecha et al.
Journal of Applied Genetics
Chromosomal and Genetic Variations
article

Maize chromatin introgression’s effect in oat × maize addition lines

Edyta Skrzypek, Mahmoud Said, Marzena Warchoł, Tomasz Warzecha, Aleš Pečinka, Anna Nowicka, Dominika Idziak-Helmcke, Katarzyna Juzoń
article en

Abstract

The addition lines derived from oat (Avena sativa L.) × maize (Zea mays L.) crosses constitute a unique tool for studying gene expression and the structure of chromatin, as well as a source of agronomically desirable traits in the context of new intergeneric hybrid cultivars. Therefore, for a better understanding of the introgression of maize chromatin into the oat genome, a comprehensive analysis of oat × maize lines was conducted. The presence of maize chromatin was confirmed in three tested lines by PCR-based amplification of the maize retrotransposon Grande-1, and verified by genomic in situ hybridization. Interestingly, the addition lines containing cytologically-detectable maize chromosomes showed a possible disturbance of the Rabl-like centromere-telomere polarization typical for oat. Moreover, the maize chromatin was consistently positioned near the nuclear periphery. The maize chromatin introgression caused a prolonged DNA replication phase, altering cell cycle dynamics, and may led to mitotic abnormalities, such as the formation of micronuclei and anaphase chromosome bridges. The introgression lines also showed morphological and physiological changes: smaller seeds, hampered seedlings' growth, and reduced yield parameters (number of flowers/seeds per plant/panicle and seed weight). These findings shed more light on the consequences of the maize chromatin introgression into the oat genome and the stability and utility of the obtained hybrids.

Journal of Applied Genetics
University of Agriculture in Krakow (PL), Franciszek Górski Institute of Plant Physiology (PL), Czech Academy of Sciences, Institute of Experimental Botany (CZ), Agricultural Research Center (EG), University of Silesia in Katowice (PL), Polish Academy of Sciences (PL)
Ministerstvo Školství, Mládeže a Tělovýchovy, Narodowe Centrum Nauki, Narodowym Centrum Nauki
Zero hunger
Openalex Percentile: Top 9%
Chromosomal and Genetic Variations
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