Xu Zhongping, Wang Guanying, Zhu Xiangqian, Wang Ruipeng, Zhu Longfu, Tu Lili, Liu Yuling, Peng Renhai, Lindsey Keith, Wang Maojun, Zhang Xianlong, Jin Shuangxia
National Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Research Base, Anyang Institute of Technology, State Key Laboratory of Cotton Biology, Anyang, China.
Nat Genet. 2025 Jul 22. doi: 10.1038/s41588-025-02258-3.
Somatic embryogenesis is crucial for plant genetic engineering, yet the underlying mechanisms in cotton remain poorly understood. Here we present a telomere-to-telomere assembly of Jin668 and a high-quality assembly of YZ1, two highly regenerative allotetraploid cotton germplasms. The completion of the Jin668 genome enables characterization of ~30.1 Mb of centromeric regions invaded by centromeric retrotransposon of maize and Tekay retrotransposons, an ~8.1 Mb 5S rDNA array containing 25,190 copies and a ~75.1 Mb major 45S rDNA array with 8,131 copies. Comparative analyses of regenerative and recalcitrant genotypes reveal dynamic transcriptional patterns and chromatin accessibility during the initial regeneration process. A hierarchical gene regulatory network identifies AGL15 as a contributor to regeneration. Additionally, we demonstrate that genetic variation affects sgRNA target sites, while the Jin668 genome assembly reduces the risk of off-target effects in CRISPR-based genome editing. Together, the complete Jin668 genome reveals the complexity of genomic regions and cotton regeneration, and improves the precision of genome editing.
体细胞胚胎发生对于植物基因工程至关重要,但棉花中其潜在机制仍知之甚少。在此,我们展示了两个高度可再生的异源四倍体棉花种质——晋668的端粒到端粒组装以及YZ1的高质量组装。晋668基因组的完成使得能够对约30.1 Mb被玉米着丝粒反转录转座子和特卡伊反转录转座子侵入的着丝粒区域、一个包含25,190个拷贝的约8.1 Mb 5S rDNA阵列以及一个包含8,131个拷贝的约75.1 Mb主要45S rDNA阵列进行表征。对可再生和难再生基因型的比较分析揭示了初始再生过程中动态的转录模式和染色质可及性。一个分层的基因调控网络确定AGL15是再生的一个促成因素。此外,我们证明遗传变异会影响sgRNA靶位点,而晋668基因组组装降低了基于CRISPR的基因组编辑中脱靶效应的风险。总之,完整的晋668基因组揭示了基因组区域和棉花再生的复杂性,并提高了基因组编辑的精度。