scholarly journals Identification of novel cis ‐elements bound by BplMYB46 involved in abiotic stress responses and secondary wall deposition

2018 ◽  
Vol 60 (10) ◽  
pp. 1000-1014 ◽  
Author(s):  
Huiyan Guo ◽  
Liuqiang Wang ◽  
Chuanping Yang ◽  
Yiming Zhang ◽  
Chunrui Zhang ◽  
...  
Keyword(s):  
Abiotic Stress ◽  
Stress Responses ◽  
Secondary Wall ◽  
Cis Elements ◽  
Wall Deposition ◽  
Secondary Wall Deposition

Phenological Comparison of the Onset of Vessel Formation Between Ring-Porous and Diffuse-Porous Deciduous Trees in a Japanese Temperate Forest

IAWA Journal ◽  
1996 ◽  
Vol 17 (4) ◽  
pp. 431-444 ◽  
Author(s):  
Mitsuo Suzuki ◽  
Kiyotsugu Yoda ◽  
Hitoshi Suzuki
Keyword(s):  
Secondary Wall ◽  
Leaf Expansion ◽  
Vessel Element ◽  
Early Maturation ◽  
Vessel Formation ◽  
Wall Deposition ◽  
Water Conduction ◽  
Vessel Elements ◽  
Secondary Wall Deposition ◽  
Diffuse Porous

Initiation of vessel formation and vessel maturation indicated by secondary wall deposition have been compared in eleven deciduous broadleaved tree species. In ring-porous species the first vessel element formation in the current growth ring was initiated two to six weeks prior to the onset of leaf expansion, and secondary wall deposition on the vessel elements was completed from one week before to three weeks after leaf expansion. In diffuse-porous species, the first vessel element formation was initiated two to seven weeks after the onset of leaf expansion, and secondary wall deposition was completed four to nine weeks after leaf expansion. These results suggest that early maturation of the first vessel elements in the ring-porous species will serve for water conduction in early spring. On the contrary, the late maturation of the first vessel elements in the diffuse-porous species indicates that no new functional vessels exist at the time of the leaf expansion.

scholarly journals Is size an issue of time? Relationship between the duration of xylem development and cell traits

2019 ◽  
Vol 123 (7) ◽  
pp. 1257-1265 ◽  
Author(s):  
Valentina Buttò ◽  
Sergio Rossi ◽  
Annie Deslauriers ◽  
Hubert Morin
Keyword(s):  
Cell Wall ◽  
Cell Differentiation ◽  
Tree Ring ◽  
Wall Thickness ◽  
Secondary Wall ◽  
Temporal Dynamics ◽  
Secondary Growth ◽  
Growth Equation ◽  
Wall Deposition ◽  
Secondary Wall Deposition

Abstract Background and Aims Secondary growth is a process related to the formation of new cells that increase in size and wall thickness during xylogenesis. Temporal dynamics of wood formation influence cell traits, in turn affecting cell patterns across the tree ring. We verified the hypothesis that cell diameter and cell wall thickness are positively correlated with the duration of their differentiation phases. Methods Histological sections were produced by microcores to assess the periods of cell differentiation in black spruce [Picea mariana (Mill.) B.S.P.]. Samples were collected weekly between 2002 and 2016 from a total of 50 trees in five sites along a latitudinal gradient in Quebec (Canada). The intra-annual temporal dynamics of cell differentiation were estimated at a daily scale, and the relationships between cell traits and duration of differentiation were fitted using a modified von Bertalanffy growth equation. Key Results At all sites, larger cell diameters and cell wall thicknesses were observed in cells that experienced a longer period of differentiation. The relationship was a non-linear, decreasing trend that occasionally resulted in a clear asymptote. Overall, secondary wall deposition lasted longer than cell enlargement. Earlywood cells underwent an enlargement phase that lasted for 12 d on average, while secondary wall thickness lasted 15 d. Enlargement in latewood cells averaged 7 d and secondary wall deposition occurred over an average of 27 d. Conclusions Cell size across the tree ring is closely connected to the temporal dynamics of cell formation. Similar relationships were observed among the five study sites, indicating shared xylem formation dynamics across the entire latitudinal distribution of the species.The duration of cell differentiation is a key factor involved in cell growth and wall thickening of xylem, thereby determining the spatial variation of cell traits across the tree ring.

scholarly journals Overexpression of walldof transcription factor increases secondary wall deposition and alters carbon partitioning in poplar

2011 ◽  
Vol 5 (S7) ◽  
Author(s):  
Isabel R Gerhardt ◽  
Silvia B Filippi ◽  
Vagner Okura ◽  
Jaime Coutinho ◽  
Ana P Rizzato ◽  
...  
Keyword(s):  
Transcription Factor ◽  
Secondary Wall ◽  
Carbon Partitioning ◽  
Wall Deposition ◽  
Secondary Wall Deposition

scholarly journals Mutations of Arabidopsis TBL32 and TBL33 Affect Xylan Acetylation and Secondary Wall Deposition

PLoS ONE ◽  
2016 ◽  
Vol 11 (1) ◽  
pp. e0146460 ◽  
Author(s):  
Youxi Yuan ◽  
Quincy Teng ◽  
Ruiqin Zhong ◽  
Marziyeh Haghighat ◽  
Elizabeth A. Richardson ◽  
...  
Keyword(s):  
Secondary Wall ◽  
Wall Deposition ◽  
Secondary Wall Deposition

scholarly journals Identification and Characterization of the APX Gene Family and Its Expression Pattern under Phytohormone Treatment and Abiotic Stress in Populus trichocarpa

Genes ◽  
2021 ◽  
Vol 12 (3) ◽  
pp. 334
Author(s):  
Xue Leng ◽  
Hanzeng Wang ◽  
Shuang Zhang ◽  
Chunpu Qu ◽  
Chuanping Yang ◽  
...  
Keyword(s):  
Abiotic Stress ◽  
Gene Family ◽  
Stress Responses ◽  
Expression Profiles ◽  
Populus Trichocarpa ◽  
Ammonium Concentration ◽  
Cis Elements ◽  
Specific Expression ◽  
Real Time Quantitative Pcr ◽  
Gene Structures

Ascorbate peroxidase (APX) is a member of class I of the heme-containing peroxidase family. The enzyme plays important roles in scavenging reactive oxygen species for protection against oxidative damage and maintaining normal plant growth and development, as well as in biotic stress responses. In this study, we identified 11 APX genes in the Populus trichocarpa genome using bioinformatic methods. Phylogenetic analysis revealed that the PtrAPX proteins were classifiable into three clades and the members of each clade shared similar gene structures and motifs. The PtrAPX genes were distributed on six chromosomes and four segmental-duplicated gene pairs were identified. Promoter cis-elements analysis showed that the majority of PtrAPX genes contained a variety of phytohormone- and abiotic stress-related cis-elements. Tissue-specific expression profiles indicated that the PtrAPX genes primarily function in roots and leaves. Real-time quantitative PCR (RT-qPCR) analysis indicated that PtrAPX transcription was induced in response to drought, salinity, high ammonium concentration, and exogenous abscisic acid treatment. These results provide important information on the phylogenetic relationships and functions of the APX gene family in P. trichocarpa.

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