Paternally imprinted LATE‐FLOWERING2 transcription factor contributes to paternal‐excess interploidy hybridization barriers in wheat

Author:

Yang Guanghui1ORCID,Feng Man1ORCID,Yu Kuohai1ORCID,Cui Guangxian1ORCID,Zhou Yan1ORCID,Sun Lv1ORCID,Gao Lulu1ORCID,Zhang Yumei2ORCID,Peng Huiru1ORCID,Yao Yingyin1ORCID,Hu Zhaorong1ORCID,Rossi Vincenzo3ORCID,De Smet Ive45ORCID,Ni Zhongfu1ORCID,Sun Qixin1ORCID,Xin Mingming1ORCID

Affiliation:

1. State Key Laboratory for Agrobiotechnology, Key Laboratory of Crop Heterosis Utilization (MOE), Beijing Key Laboratory of Crop Genetic Improvement China Agricultural University Beijing 100193 China

2. Qingdao Agricultural University Qingdao 266109 China

3. Council for Agricultural Research and Economics Research Centre for Cereal and Industrial Crops Bergamo 24126 Italy

4. Department of Plant Biotechnology and Bioinformatics Ghent University Ghent B‐9052 Belgium

5. VIB Center for Plant Systems Biology Ghent B‐9052 Belgium

Abstract

AbstractInterploidy hybridization between hexaploid and tetraploid genotypes occurred repeatedly during genomic introgression events throughout wheat evolution, and is commonly employed in wheat breeding programs. Hexaploid wheat usually serves as maternal parent because the reciprocal cross generates progeny with severe defects and poor seed germination, but the underlying mechanism is poorly understood. Here, we performed detailed analysis of phenotypic variation in endosperm between two interploidy reciprocal crosses arising from tetraploid (Triticum durum, AABB) and hexaploid wheat (Triticum aestivum, AABBDD). In the paternal‐ versus the maternal‐excess cross, the timing of endosperm cellularization was delayed and starch granule accumulation in the endosperm was repressed, causing reduced germination percentage. The expression profiles of genes involved in nutrient metabolism differed strongly between these endosperm types. Furthermore, expression patterns of parental alleles were dramatically disturbed in interploidy versus intraploidy crosses, leading to increased number of imprinted genes. The endosperm‐specific TaLFL2 showed a paternally imprinted expression pattern in interploidy crosses partially due to allele‐specific DNA methylation. Paternal TaLFL2 binds to and represses a nutrient accumulation regulator TaNAC019, leading to reduced storage protein and starch accumulation during endosperm development in paternal‐excess cross, as confirmed by interploidy crosses between tetraploid wild‐type and clustered regularly interspaced palindromic repeats (CRISPR) – CRISPR‐associated protein 9 generated hexaploid mutants. These findings reveal a contribution of genomic imprinting to paternal‐excess interploidy hybridization barriers during wheat evolution history and explains why experienced breeders preferentially exploit maternal‐excess interploidy crosses in wheat breeding programs.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Plant Science,General Biochemistry, Genetics and Molecular Biology,Biochemistry

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