scholarly journals Different Pathways Are Involved in Phosphate and Iron Stress-Induced Alterations of Root Epidermal Cell Development

2001 ◽  
Vol 125 (4) ◽  
pp. 2078-2084 ◽  
Author(s):  
Wolfgang Schmidt ◽  
Adam Schikora
2021 ◽  
Vol 12 ◽  
Author(s):  
Guoliang Han ◽  
Yuxia Li ◽  
Ziqi Qiao ◽  
Chengfeng Wang ◽  
Yang Zhao ◽  
...  

Plant epidermal cells, such as trichomes, root hairs, salt glands, and stomata, play pivotal roles in the growth, development, and environmental adaptation of terrestrial plants. Cell fate determination, differentiation, and the formation of epidermal structures represent basic developmental processes in multicellular organisms. Increasing evidence indicates that C2H2 zinc finger proteins play important roles in regulating the development of epidermal structures in plants and plant adaptation to unfavorable environments. Here, we systematically summarize the molecular mechanism underlying the roles of C2H2 zinc finger proteins in controlling epidermal cell formation in plants, with an emphasis on trichomes, root hairs, and salt glands and their roles in plant adaptation to environmental stress. In addition, we discuss the possible roles of homologous C2H2 zinc finger proteins in trichome development in non-halophytes and salt gland development in halophytes based on bioinformatic analysis. This review provides a foundation for further study of epidermal cell development and abiotic stress responses in plants.


2018 ◽  
Vol 433 (2) ◽  
pp. 357-373 ◽  
Author(s):  
Li-Chun Cheng ◽  
Kimberly C. Tu ◽  
Chris W. Seidel ◽  
Sofia M.C. Robb ◽  
Fengli Guo ◽  
...  

1981 ◽  
Vol 21 (3) ◽  
pp. 751-762 ◽  
Author(s):  
LYNN M. RIDDIFORD

2020 ◽  
Vol 103 (6) ◽  
pp. 609-621 ◽  
Author(s):  
Kuanqiang Tang ◽  
Suxin Yang ◽  
Xingxing Feng ◽  
Tao Wu ◽  
Jiantian Leng ◽  
...  

2021 ◽  
Author(s):  
Hsiang-Chia Lu ◽  
Sio-Hong Lam ◽  
Diyang Zhang ◽  
Yu-Yun Hsiao ◽  
Bai-Jun Li ◽  
...  

Abstract Petals of the monocot Phalaenopsis aphrodite (Orchidaceae) possess conical epidermal cells on their adaxial surfaces, and a large amount of cuticular wax is deposited on them to serve as a primary barrier against biotic and abiotic stresses. It has been widely reported that subgroup 9A members of the R2R3-MYB gene family, MIXTA and MIXTA-like in eudicots, act to regulate the differentiation of conical epidermal cells. However, the molecular pathways underlying conical epidermal cell development and cuticular wax biosynthesis in monocot petals remain unclear. Here, we characterized two subgroup 9A R2R3-MYB genes, PaMYB9A1 and PaMYB9A2 (PaMYB9A1/2), from P. aphrodite through the transient overexpression of their coding sequences and corresponding chimeric repressors in developing petals. We showed that PaMYB9A1/2 function to coordinate conical epidermal cell development and cuticular wax biosynthesis. In addition, we identified putative targets of PaMYB9A1/2 through comparative transcriptome analyses, revealing that PaMYB9A1/2 act to regulate the expression of cell wall-associated and wax biosynthetic genes. Furthermore, a chemical composition analysis of cuticular wax showed that even-chain n-alkanes and odd-chain primary alcohols are the main chemical constituents of cuticular wax deposited on petals, which is inconsistent with the well-known biosynthetic pathways of cuticular wax, implying a distinct biosynthetic pathway occurring in P. aphrodite flowers. These results reveal that the function of subgroup 9A R2R3-MYB family genes in regulating the differentiation of epidermal cells is largely conserved in monocots and dicots. Furthermore, both PaMYB9A1/2 have evolved additional functions controlling the biosynthesis of cuticular wax.


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