College of Life Sciences, Wuhan University, Wuhan 430072, China.
State Key Laboratory of Plant Genomics and National Center for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
Plant Commun. 2024 Oct 14;5(10):101003. doi: 10.1016/j.xplc.2024.101003. Epub 2024 Jun 13.
E3 ligases are key enzymes required for protein degradation. Here, we identified a C3H2C3 RING domain-containing E3 ubiquitin ligase gene named GhATL68b. It is preferentially and highly expressed in developing cotton fiber cells and shows greater conservation in plants than in animals or archaea. The four orthologous copies of this gene in various diploid cottons and eight in the allotetraploid G. hirsutum were found to have originated from a single common ancestor that can be traced back to Chlamydomonas reinhardtii at about 992 million years ago. Structural variations in the GhATL68b promoter regions of G. hirsutum, G. herbaceum, G. arboreum, and G. raimondii are correlated with significantly different methylation patterns. Homozygous CRISPR-Cas9 knockout cotton lines exhibit significant reductions in fiber quality traits, including upper-half mean length, elongation at break, uniformity, and mature fiber weight. In vitro ubiquitination and cell-free protein degradation assays revealed that GhATL68b modulates the homeostasis of 2,4-dienoyl-CoA reductase, a rate-limiting enzyme for the β-oxidation of polyunsaturated fatty acids (PUFAs), via the ubiquitin proteasome pathway. Fiber cells harvested from these knockout mutants contain significantly lower levels of PUFAs important for production of glycerophospholipids and regulation of plasma membrane fluidity. The fiber growth defects of the mutant can be fully rescued by the addition of linolenic acid (C18:3), the most abundant type of PUFA, to the ovule culture medium. This experimentally characterized C3H2C3 type E3 ubiquitin ligase involved in regulating fiber cell elongation may provide us with a new genetic target for improved cotton lint production.
E3 连接酶是蛋白质降解所必需的关键酶。在这里,我们鉴定了一个 C3H2C3 RING 结构域包含的 E3 泛素连接酶基因,命名为 GhATL68b。它在发育中的棉花纤维细胞中优先且高度表达,在植物中的保守性大于动物或古菌。在各种二倍体棉和八倍体 G. hirsutum 中发现了该基因的四个直系同源物,它们都起源于大约 9.92 亿年前可以追溯到莱茵衣藻的单个共同祖先。GhATL68b 启动子区域的结构变异与 G. hirsutum、G. herbaceum、G. arboreum 和 G. raimondii 中的显著不同的甲基化模式相关。CRISPR-Cas9 同源敲除棉花品系的纯合子表现出纤维质量特性的显著降低,包括上半部分平均长度、断裂伸长率、均匀性和成熟纤维重量。体外泛素化和无细胞蛋白降解测定显示,GhATL68b 通过泛素蛋白酶体途径调节 2,4-二烯酰基辅酶 A 还原酶的动态平衡,2,4-二烯酰基辅酶 A 还原酶是多不饱和脂肪酸 (PUFA) β-氧化的限速酶。从这些敲除突变体中收获的纤维细胞含有对甘油磷脂合成和质膜流动性调节很重要的 PUFAs 水平显著降低。在胚珠培养基中添加亚油酸(C18:3)(最丰富的 PUFAs 类型)可完全挽救突变体的纤维生长缺陷。这种经过实验鉴定的参与调节纤维细胞伸长的 C3H2C3 型 E3 泛素连接酶可能为提高棉花 lint 产量提供了新的遗传靶标。