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

IF 9.3 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Integrative Plant Biology Pub Date : 2023-12-01 Epub Date: 2023-11-17 DOI:10.1111/jipb.13574
Guanghui Yang, Man Feng, Kuohai Yu, Guangxian Cui, Yan Zhou, Lv Sun, Lulu Gao, Yumei Zhang, Huiru Peng, Yingyin Yao, Zhaorong Hu, Vincenzo Rossi, Ive De Smet, Zhongfu Ni, Qixin Sun, Mingming Xin
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Abstract

Interploidy 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.

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小麦父系印迹LATE-FLOWERING2转录因子导致父系过量多倍体间杂交障碍。
在整个小麦进化过程中,六倍体和四倍体基因型之间的多倍体杂交在基因组渗入事件中反复发生,并且通常用于小麦育种计划。六倍体小麦通常作为母本,因为互惠杂交产生的后代具有严重缺陷和不良种子发芽,但其潜在机制尚不清楚。在这里,我们对四倍体小麦(硬粒小麦,AABB)和六倍体小麦(普通小麦,AABBDD)的两个倍间互惠杂交之间胚乳的表型变异进行了详细分析。在父系与母系过量杂交中,胚乳细胞化的时间被推迟,淀粉颗粒在胚乳中的积累被抑制,导致发芽率降低。参与营养代谢的基因在这些胚乳类型之间的表达谱差异很大。此外,亲本等位基因的表达模式在染色体间杂交与染色体内杂交中受到显著干扰,导致印迹基因数量增加。胚乳特异性TaLFL2在倍体间杂交中表现出父系印迹表达模式,部分原因是等位基因特异性DNA甲基化。父系TaLFL2与营养积累调节剂TaNAC019结合并抑制,导致父系过量杂交中胚乳发育过程中储存蛋白和淀粉积累减少,四倍体野生型和CRISPR-Cas9产生的六倍体突变体之间的多倍体杂交证实了这一点。这些发现揭示了基因组印迹在小麦进化史上对父系过量倍性杂交障碍的贡献,并解释了为什么有经验的育种家在小麦育种计划中优先利用母系过量倍间杂交。这篇文章受版权保护。保留所有权利。
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来源期刊
Journal of Integrative Plant Biology
Journal of Integrative Plant Biology 生物-生化与分子生物学
CiteScore
18.00
自引率
5.30%
发文量
220
审稿时长
3 months
期刊介绍: Journal of Integrative Plant Biology is a leading academic journal reporting on the latest discoveries in plant biology.Enjoy the latest news and developments in the field, understand new and improved methods and research tools, and explore basic biological questions through reproducible experimental design, using genetic, biochemical, cell and molecular biological methods, and statistical analyses.
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