scholarly journals Metabolic and Physical Control of Cell Elongation Rate

1971 ◽  
Vol 47 (3) ◽  
pp. 423-430 ◽  
Author(s):  
P. B. Green ◽  
R. O. Erickson ◽  
J. Buggy
Keyword(s):  
Cell Elongation ◽  
Elongation Rate ◽  
Physical Control

Epidermal cell division and cell elongation in two Aegilops species with contrasting leaf elongation rates

2003 ◽  
Vol 30 (4) ◽  
pp. 425 ◽  
Author(s):  
Lieve Bultynck ◽  
Fabio Fiorani ◽  
Elizabeth Van Volkenburgh ◽  
Hans Lambers
Keyword(s):  
Cell Division ◽  
Cell Elongation ◽  
Aegilops Tauschii ◽  
Growth Zone ◽  
Elongation Rate ◽  
Main Stem ◽  
Leaf Number ◽  
Leaf Elongation ◽  
Division Rate ◽  
Dividing Cells

The 2-fold difference in final length of leaf number three on the main stem between the fast-growing Aegilops tauschii L. and the slow-growing Aegilops caudata L. is correlated with a difference in leaf elongation rate (LER), and not in duration of leaf elongation. In this paper the cellular basis of inherent differences in LER between these species was investigated.The dynamics of abaxial epidermal cells along the growth zone of leaf number three on the main stem of both species was analysed by means of a kinematic analysis. The faster LER of Ae. tauschii compared with that of Ae.�caudata was associated with (i) a larger leaf basal meristem and cell elongation-only zone, and (ii) a faster cell production rate owing to a larger number of dividing cells. Cell division rate, mature cell size and cell elongation rate did not differ between the two species. The lack of variation in cell expansion rate between the species was supported by a similar capacity of both species to extend their isolated cell walls upon acidification.These data suggest that differences in the number of dividing cells can bring about differences in the number of simultaneously elongating cells, and hence in LER.

Primary Root Elongation Rate and Abscisic Acid Levels of Maize in Response to Water Stress

Crop Science ◽  
2011 ◽  
Vol 51 (1) ◽  
pp. 157-172 ◽  
Author(s):  
Kristen A. Leach ◽  
Lindsey G. Hejlek ◽  
Leonard B. Hearne ◽  
Henry T. Nguyen ◽  
Robert E. Sharp ◽  
...  
Keyword(s):  
Abscisic Acid ◽  
Water Stress ◽  
Root Elongation ◽  
Primary Root ◽  
Elongation Rate ◽  
Root Elongation Rate ◽  
Response To Water

scholarly journals Slm9, a Novel Nuclear Protein Involved in Mitotic Control in Fission Yeast

Genetics ◽  
2000 ◽  
Vol 155 (2) ◽  
pp. 623-631
Author(s):  
Junko Kanoh ◽  
Paul Russell
Keyword(s):  
Cell Cycle ◽  
Fission Yeast ◽  
Cell Elongation ◽  
Nuclear Protein ◽  
G1 Arrest ◽  
Permissive Temperature ◽  
Cdc2 Kinase ◽  
Synthetic Lethal ◽  
Cycle Arrest ◽  
Novel Protein

Abstract In the fission yeast Schizosaccharomyces pombe, as in other eukaryotic cells, Cdc2/cyclin B complex is the key regulator of mitosis. Perhaps the most important regulation of Cdc2 is the inhibitory phosphorylation of tyrosine-15 that is catalyzed by Wee1 and Mik1. Cdc25 and Pyp3 phosphatases dephosphorylate tyrosine-15 and activate Cdc2. To isolate novel activators of Cdc2 kinase, we screened synthetic lethal mutants in a cdc25-22 background at the permissive temperature (25°). One of the genes, slm9, encodes a novel protein of 807 amino acids. Slm9 is most similar to Hir2, the histone gene regulator in budding yeast. Slm9 protein level is constant and Slm9 is localized to the nucleus throughout the cell cycle. The slm9 disruptant is delayed at the G2-M transition as indicated by cell elongation and analysis of DNA content. Inactivation of Wee1 fully suppressed the cell elongation phenotype caused by the slm9 mutation. The slm9 mutant is defective in recovery from G1 arrest after nitrogen starvation. The slm9 mutant is also UV sensitive, showing a defect in recovery from the cell cycle arrest after UV irradiation.

scholarly journals Transcriptome and metabolome profiling provide insights into molecular mechanism of pseudostem elongation in banana

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Guiming Deng ◽  
Fangcheng Bi ◽  
Jing Liu ◽  
Weidi He ◽  
Chunyu Li ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Elongation ◽  
Molecular Mechanisms ◽  
Specific Gene ◽  
Wild Type ◽  
Banana Plant ◽  
Cell Wall Modification ◽  
Dwarf Cultivar ◽  
Important Trait ◽  
Metabolome Profiling

AbstractBackgroundBanana plant height is an important trait for horticultural practices and semi-dwarf cultivars show better resistance to damages by wind and rain. However, the molecular mechanisms controlling the pseudostem height remain poorly understood. Herein, we studied the molecular changes in the pseudostem of a semi-dwarf banana mutant Aifen No. 1 (Musaspp. Pisang Awak sub-group ABB) as compared to its wild-type dwarf cultivar using a combined transcriptome and metabolome approach.ResultsA total of 127 differentially expressed genes and 48 differentially accumulated metabolites were detected between the mutant and its wild type. Metabolites belonging to amino acid and its derivatives, flavonoids, lignans, coumarins, organic acids, and phenolic acids were up-regulated in the mutant. The transcriptome analysis showed the differential regulation of genes related to the gibberellin pathway, auxin transport, cell elongation, and cell wall modification. Based on the regulation of gibberellin and associated pathway-related genes, we discussed the involvement of gibberellins in pseudostem elongation in the mutant banana. Genes and metabolites associated with cell wall were explored and their involvement in cell extension is discussed.ConclusionsThe results suggest that gibberellins and associated pathways are possibly developing the observed semi-dwarf pseudostem phenotype together with cell elongation and cell wall modification. The findings increase the understanding of the mechanisms underlying banana stem height and provide new clues for further dissection of specific gene functions.

Sign in / Sign up

Export Citation Format

Share Document