Abstract: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 en… Show more
“…Therefore, within one week of infection by ARD-associated F. proliferatum MR5, the roots of M26 and T337 showed numerous brown spots, rot, and fractures (Figure 2). These observations were consistent with previous reports of epidermal cell lysis, disintegration of cortical cells, root tip necrosis, and the almost complete loss of functional root hairs due to excessive accumulation of reactive oxygen species (Petrov et al, 2015;Han et al, 2021). Unlike the other two rootstocks, 12-2 could maintain a degree of balance between ROS production and scavenging, thereby maintaining the normal cellular redox state (Tanveer and Shah, 2017).…”
The cultivation of resistant rootstocks is one of the more effective ways to mitigate apple replant disease (ARD). We performed an ion current test, a pot experiment, and a pathogen infection test on the apple rootstocks 12-2 (self-named), T337, and M26. The ion current test showed that exposure to ARD soil extract for 30 min had a significant effect on K+ ion currents at the meristem, elongation, and mature zones of the M26 rhizoplane and on Ca2+ currents in the meristem and elongation zones. ARD also had a significant effect on Ca2+ currents in the meristem, elongation, and mature zones of the T337 rhizoplane. Exposure to ARD soil extract for 5 min had a significant effect on K+ currents in the meristem, elongation, and mature zones of 12-2 and on the Ca2+ currents in the elongation and mature zones. Compared to a 5-min exposure, a 30-min exposure to ARD extract had a less pronounced effect on K+ and Ca2+ currents in the 12-2 rhizoplane. The pot experiment showed that ARD soil had no significant effect on any root architectural or physiological parameters of 12-2. By contrast, ARD soil significantly reduced some root growth indices and the dry and fresh weights of T337 and M26 compared with controls on sterilized soil. ARD also had a significant effect on root metabolic activity, root antioxidant enzyme activity (except superoxide dismutase for T337), and malondialdehyde content of T337 and M26. Pathogen infection tests showed that Fusarium proliferatum MR5 significantly affected the root structure and reduced the root metabolic activity of T337 and M26. It also reduced their root antioxidant enzyme activities (except catalase for T337) and significantly increased the root malondialdehyde content, reactive oxygen levels, and proline and soluble sugar contents. By contrast, MR5 had no such effects on 12-2. Based on these results, 12-2 has the potential to serve as an important ARD-resistant rootstock.
“…Therefore, within one week of infection by ARD-associated F. proliferatum MR5, the roots of M26 and T337 showed numerous brown spots, rot, and fractures (Figure 2). These observations were consistent with previous reports of epidermal cell lysis, disintegration of cortical cells, root tip necrosis, and the almost complete loss of functional root hairs due to excessive accumulation of reactive oxygen species (Petrov et al, 2015;Han et al, 2021). Unlike the other two rootstocks, 12-2 could maintain a degree of balance between ROS production and scavenging, thereby maintaining the normal cellular redox state (Tanveer and Shah, 2017).…”
The cultivation of resistant rootstocks is one of the more effective ways to mitigate apple replant disease (ARD). We performed an ion current test, a pot experiment, and a pathogen infection test on the apple rootstocks 12-2 (self-named), T337, and M26. The ion current test showed that exposure to ARD soil extract for 30 min had a significant effect on K+ ion currents at the meristem, elongation, and mature zones of the M26 rhizoplane and on Ca2+ currents in the meristem and elongation zones. ARD also had a significant effect on Ca2+ currents in the meristem, elongation, and mature zones of the T337 rhizoplane. Exposure to ARD soil extract for 5 min had a significant effect on K+ currents in the meristem, elongation, and mature zones of 12-2 and on the Ca2+ currents in the elongation and mature zones. Compared to a 5-min exposure, a 30-min exposure to ARD extract had a less pronounced effect on K+ and Ca2+ currents in the 12-2 rhizoplane. The pot experiment showed that ARD soil had no significant effect on any root architectural or physiological parameters of 12-2. By contrast, ARD soil significantly reduced some root growth indices and the dry and fresh weights of T337 and M26 compared with controls on sterilized soil. ARD also had a significant effect on root metabolic activity, root antioxidant enzyme activity (except superoxide dismutase for T337), and malondialdehyde content of T337 and M26. Pathogen infection tests showed that Fusarium proliferatum MR5 significantly affected the root structure and reduced the root metabolic activity of T337 and M26. It also reduced their root antioxidant enzyme activities (except catalase for T337) and significantly increased the root malondialdehyde content, reactive oxygen levels, and proline and soluble sugar contents. By contrast, MR5 had no such effects on 12-2. Based on these results, 12-2 has the potential to serve as an important ARD-resistant rootstock.
“…Two Cys and two His form coordination bonds with zinc atoms, which generate a stable finger-like structure [ 6 ]. The finger-like structure extends into the large groove of DNA double helix and specific contacts with DNA bases, so that it is capable of playing a role in transcriptional regulation [ 3 , 6 ]. In this finger-like structure, each finger domain contains one α-helix in the C-terminal and two β-strands in its N-terminal, creating a relatively independent structure.…”
Section: Structure and Classification Of C2h2-zfpsmentioning
confidence: 99%
“…The zinc finger proteins (ZFPs), named from the 'finger-like' zinc finger, are one of the largest families of transcription factors and are abundantly distributed in the plant kingdom [1][2][3][4]. ZFPs harbor a highly conserved domain which consists of approximately 20-30 amino acid residues with a consensus sequence of CX2-4CX3FX5LX2HX3-5H (X represents any amino acid, subscript: the number of amino acid) [1,2,5].…”
Section: Introductionmentioning
confidence: 99%
“…As diverse as zinc finger proteins' functions are, their structures are also varied and divided into different classes according to the numbers and positions of the cysteine (Cys) and histidine (His) residues that bind the zinc ion [6]. Based on this canonical classification method of zinc finger proteins, the members of these classes include C2H2 (TFIIIA), C2HC (Retroviral nucleocapsid), C2HC5 (LIM domain), C2C2, C3HC4 (RING finger), C4 (GATA-1), C4HC3 (Requium), C6 (GAL4), and other classes [3,6,8,9]. Among these subclasses, the C2H2 zinc finger proteins contain one of the best-characterized DNA-binding motifs, which are composed of two Cys and two His residues together with one zinc ion tetrahedrally [2,6].…”
Section: Introductionmentioning
confidence: 99%
“…In Arabidopsis thaliana, 176 C2H2-ZFPs have been reported, and 189, 109, 321, 118 and 47 C2H2-type ZFPs have been identified in rice (Oryza sativa), poplar (Populus trichocarpa), soybean (Glycine max), tobacco (Nicotiana tabacum) and wheat (Triticum aestivum), respectively [10][11][12][13][14]. Function analyses showed that C2H2-ZFPs are involved in regulating multiple growth development processes and resisting biotic and abiotic stress in plants [2][3][4]15].…”
Abiotic stresses have already exhibited the negative effects on crop growth and development, thereby influencing crop quality and yield. Therefore, plants have developed regulatory mechanisms to adopt against such harsh changing environmental conditions. Recent studies have shown that zinc finger protein transcription factors play a crucial role in plant growth and development as well as in stress response. C2H2 zinc finger proteins are one of the best-studied types and have been shown to play diverse roles in the plant abiotic stress responses. However, the C2H2 zinc finger network in plants is complex and needs to be further studied in abiotic stress responses. Here in this review, we mainly focus on recent findings on the regulatory mechanisms, summarize the structural and functional characterization of C2H2 zinc finger proteins, and discuss the C2H2 zinc finger proteins involved in the different signal pathways in plant responses to abiotic stress.
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