Jianwei Gu, Jiayin Chen, Chenqi Zhao, Dengfeng Hong
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The BnaEOD1.A04 showed a similar type of editing in these mutants, whereas the BnaEOD1.C04 in T<sub>2</sub>-397-2-E2 was only missing 26 amino acids, and the translation was not prematurely terminated, which was different from the other two mutants. In parallel, mutation of <i>BnaEOD1s</i> resulted in a noteworthy increase in both seed size and seed weight in the three editing lines. Additionally, there was a significant decline in the number of seeds per silique (SPS) and silique length (SL) in T<sub>2</sub>-157-1-C8 and T<sub>2</sub>-390-2-B8, but T<sub>2</sub>-397-2-E2 did not show any significant changes in the SPS and SL, possibly due to distinct types of editing in the three lines. The above results indicate the conserved function of <i>EOD1</i> homologs and provides promising germplasm for breeding novel high-yield rapeseed varieties by improving seed size and thousand-seed weight.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s11032-023-01430-z.</p>","PeriodicalId":18769,"journal":{"name":"Molecular Breeding","volume":"43 11","pages":"79"},"PeriodicalIF":2.6000,"publicationDate":"2023-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632315/pdf/","citationCount":"0","resultStr":"{\"title\":\"Mutating <i>BnEOD1s</i> via CRISPR-Cas9 increases the seed size and weight in <i>Brassica napus</i>.\",\"authors\":\"Jianwei Gu, Jiayin Chen, Chenqi Zhao, Dengfeng Hong\",\"doi\":\"10.1007/s11032-023-01430-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Seed weight, which is highly correlated to seed size, is a critical agronomic trait that determines the yield of <i>Brassica napus.</i> However, there have been limited researches on the genes involved in regulating seed size. In <i>Arabidopsis thaliana</i>, <i>ENHANCER OF DA1</i> (<i>EOD1</i>), an E3 ubiquitin ligase gene, has been identified as a significant negative regulator in controlling organ size, but the function of its homologs in rapeseed remains unknown. Only two homologous of <i>EOD1</i>, <i>BnaEOD1.A04 and BnaEOD1.C04</i>, have been found in <i>B. napus</i> and were mutated using the CRISPR-Cas9 system. Three T-DNA-free lines, T<sub>2</sub>-157-1-C8, T<sub>2</sub>-390-2-B8, and T<sub>2</sub>-397-2-E2, were identified from the homozygous T<sub>2</sub> mutant lines. The BnaEOD1.A04 showed a similar type of editing in these mutants, whereas the BnaEOD1.C04 in T<sub>2</sub>-397-2-E2 was only missing 26 amino acids, and the translation was not prematurely terminated, which was different from the other two mutants. In parallel, mutation of <i>BnaEOD1s</i> resulted in a noteworthy increase in both seed size and seed weight in the three editing lines. 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引用次数: 0
摘要
籽粒重是决定甘蓝型油菜产量的关键农艺性状,籽粒重与籽粒大小高度相关。然而,关于调控种子大小的基因研究有限。在拟南芥中,E3泛素连接酶基因DA1的增强子(ENHANCER OF DA1, EOD1)已被确定为控制器官大小的显著负调控因子,但其同源物在油菜籽中的功能尚不清楚。只有两个EOD1的同源物,BnaEOD1。A04和BnaEOD1。在甘蓝型酵母中发现了C04,并使用CRISPR-Cas9系统进行了突变。从T2纯合子突变系中鉴定出T2-157-1- c8、T2-390-2- b8和T2-397-2- e2 3个无t - dna系。BnaEOD1。A04在这些突变体中显示出类似的编辑类型,而BnaEOD1。T2-397-2-E2中的C04仅缺失26个氨基酸,且没有过早终止翻译,这与其他两个突变体不同。同时,bnaeod1突变导致三个编辑系的种子大小和种子重量显著增加。此外,T2-157-1-C8和T2-390-2-B8的单株种子数(SPS)和单株长度(SL)均显著下降,而T2-397-2-E2的SPS和单株长度未发生显著变化,这可能是由于3个品系的编辑类型不同所致。上述结果说明了EOD1同源物的保守功能,为通过提高籽粒大小和千粒重来选育油菜高产新品种提供了良好的种质资源。补充资料:在线版本提供补充资料,网址为10.1007/s11032-023-01430-z。
Mutating BnEOD1s via CRISPR-Cas9 increases the seed size and weight in Brassica napus.
Seed weight, which is highly correlated to seed size, is a critical agronomic trait that determines the yield of Brassica napus. However, there have been limited researches on the genes involved in regulating seed size. In Arabidopsis thaliana, ENHANCER OF DA1 (EOD1), an E3 ubiquitin ligase gene, has been identified as a significant negative regulator in controlling organ size, but the function of its homologs in rapeseed remains unknown. Only two homologous of EOD1, BnaEOD1.A04 and BnaEOD1.C04, have been found in B. napus and were mutated using the CRISPR-Cas9 system. Three T-DNA-free lines, T2-157-1-C8, T2-390-2-B8, and T2-397-2-E2, were identified from the homozygous T2 mutant lines. The BnaEOD1.A04 showed a similar type of editing in these mutants, whereas the BnaEOD1.C04 in T2-397-2-E2 was only missing 26 amino acids, and the translation was not prematurely terminated, which was different from the other two mutants. In parallel, mutation of BnaEOD1s resulted in a noteworthy increase in both seed size and seed weight in the three editing lines. Additionally, there was a significant decline in the number of seeds per silique (SPS) and silique length (SL) in T2-157-1-C8 and T2-390-2-B8, but T2-397-2-E2 did not show any significant changes in the SPS and SL, possibly due to distinct types of editing in the three lines. The above results indicate the conserved function of EOD1 homologs and provides promising germplasm for breeding novel high-yield rapeseed varieties by improving seed size and thousand-seed weight.
Supplementary information: The online version contains supplementary material available at 10.1007/s11032-023-01430-z.
期刊介绍:
Molecular Breeding is an international journal publishing papers on applications of plant molecular biology, i.e., research most likely leading to practical applications. The practical applications might relate to the Developing as well as the industrialised World and have demonstrable benefits for the seed industry, farmers, processing industry, the environment and the consumer.
All papers published should contribute to the understanding and progress of modern plant breeding, encompassing the scientific disciplines of molecular biology, biochemistry, genetics, physiology, pathology, plant breeding, and ecology among others.
Molecular Breeding welcomes the following categories of papers: full papers, short communications, papers describing novel methods and review papers. All submission will be subject to peer review ensuring the highest possible scientific quality standards.
Molecular Breeding core areas:
Molecular Breeding will consider manuscripts describing contemporary methods of molecular genetics and genomic analysis, structural and functional genomics in crops, proteomics and metabolic profiling, abiotic stress and field evaluation of transgenic crops containing particular traits. Manuscripts on marker assisted breeding are also of major interest, in particular novel approaches and new results of marker assisted breeding, QTL cloning, integration of conventional and marker assisted breeding, and QTL studies in crop plants.