Fine-mapping of the woolly gene controlling multicellular trichome formation and embryonic development in tomato

2011 ◽  
Vol 123 (4) ◽  
pp. 625-633 ◽  
Author(s):  
Changxian Yang ◽  
Hanxia Li ◽  
Junhong Zhang ◽  
Taotao Wang ◽  
Zhibiao Ye
2016 ◽  
Vol 129 (8) ◽  
pp. 1531-1539 ◽  
Author(s):  
Jiang Chang ◽  
Ting Yu ◽  
Shenghua Gao ◽  
Cheng Xiong ◽  
Qingmin Xie ◽  
...  

2020 ◽  
Vol 104 (1) ◽  
pp. 18-29
Author(s):  
Xiaoli Liao ◽  
Junqiang Wang ◽  
Shunhua Zhu ◽  
Qingmin Xie ◽  
Lin Wang ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Jinqiu Liu ◽  
Haoran Wang ◽  
Mengmeng Liu ◽  
Jinkui Liu ◽  
Sujun Liu ◽  
...  

Trichomes are unicellular or multicellular epidermal structures that play a defensive role against environmental stresses. Although unicellular trichomes have been extensively studied as a mechanistic model, the genes involved in multicellular trichome formation are not well understood. In this study, we first classified the trichome morphology structures in Capsicum species using 280 diverse peppers. We cloned a key gene (Hairiness) on chromosome 10, which mainly controlled the formation of multicellular non-glandular trichomes (types II, III, and V). Hairiness encodes a Cys2-His2 zinc-finger protein, and virus-induced gene silencing of the gene resulted in a hairless phenotype. Differential expression of Hairiness between the hairiness and hairless lines was due to variations in promoter sequences. Transgenic experiments verified the hypothesis that the promoter of Hairiness in the hairless line had extremely low activity causing a hairless phenotype. Hair controlled the formation of type I glandular trichomes in tomatoes, which was due to nucleotide differences. Taken together, our findings suggest that the regulation of multicellular trichome formation might have similar pathways, but the gene could perform slightly different functions in crops.


2009 ◽  
Vol 120 (6) ◽  
pp. 1099-1106 ◽  
Author(s):  
Hyun Jung Kim ◽  
Jung-Heon Han ◽  
Jin-Kyung Kwon ◽  
Minkyu Park ◽  
Byung-Dong Kim ◽  
...  

2020 ◽  
Vol 71 (22) ◽  
pp. 7132-7145
Author(s):  
Qingmin Xie ◽  
Yanna Gao ◽  
Jing Li ◽  
Qihong Yang ◽  
Xiaolu Qu ◽  
...  

Abstract Trichomes are specialized epidermal appendages that serve as excellent models to study cell morphogenesis. Although the molecular mechanism underlying trichome morphogenesis in Arabidopsis has been well characterized, most of the regulators essential for multicellular trichome morphology remain unknown in tomato. In this study, we determined that the recessive hairless-2 (hl-2) mutation in tomato causes severe distortion of all trichome types, along with increased stem fragility. Using map-based cloning, we found that the hl-2 phenotype was associated with a 100 bp insertion in the coding region of Nck-associated protein 1, a component of the SCAR/WAVE complex. Direct protein-protein interaction was detected between Hl-2 and Hl (SRA1, specifically Rac1-associated protein) using yeast two-hybrid and co-immunoprecipitation assays, suggesting that these proteins may work together during trichome formation. In addition, knock-down of a HD-Zip IV transcription factor, HDZIPIV8, distorted trichomes similar to the hl-2 mutant. HDZIPIV8 regulates the expression of Hl-2 by binding to the L1-box in the Hl-2 promoter region, and is involved in organizing actin filaments. The brittleness of hl-2 stems was found to result from decreased cellulose content. Taken together, these findings suggest that the Hl-2 gene plays an important role in controlling multicellular trichome morphogenesis and mechanical properties of stems in tomato plants.


2018 ◽  
Vol 96 (1) ◽  
pp. 90-102 ◽  
Author(s):  
Jiang Chang ◽  
Ting Yu ◽  
Qihong Yang ◽  
Changxing Li ◽  
Cheng Xiong ◽  
...  

2001 ◽  
Vol 7 (S2) ◽  
pp. 1012-1013
Author(s):  
Uyen Tram ◽  
William Sullivan

Embryonic development is a dynamic event and is best studied in live animals in real time. Much of our knowledge of the early events of embryogenesis, however, comes from immunofluourescent analysis of fixed embryos. While these studies provide an enormous amount of information about the organization of different structures during development, they can give only a static glimpse of a very dynamic event. More recently real-time fluorescent studies of living embryos have become much more routine and have given new insights to how different structures and organelles (chromosomes, centrosomes, cytoskeleton, etc.) are coordinately regulated. This is in large part due to the development of commercially available fluorescent probes, GFP technology, and newly developed sensitive fluorescent microscopes. For example, live confocal fluorescent analysis proved essential in determining the primary defect in mutations that disrupt early nuclear divisions in Drosophila melanogaster. For organisms in which GPF transgenics is not available, fluorescent probes that label DNA, microtubules, and actin are available for microinjection.


Sign in / Sign up

Export Citation Format

Share Document