» Articles » PMID: 16667937

Genetic Regulation of Development in Sorghum Bicolor: V. The Ma(3) Allele Results in Gibberellin Enrichment

Overview
Journal Plant Physiol
Specialty Physiology
Date 1991 Jan 1
PMID 16667937
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

Sorghum bicolor genotypes, near isogenic with different alleles at the third maturity locus, were compared for development, for responsiveness to GA(3) and a GA synthesis inhibitor, and occurrence and concentrations of endogenous GAs, IAA, and ABA. At 14 days the genotype 58M (ma(3) (R)ma(3) (R)) exhibited 2.5-fold greater culm height, 1.75-fold greater total height, and 1.38-fold greater dry weight than 90M (ma(3)ma(3)) or 100M (Ma(3)Ma(3)). All three genotypes exhibited similar shoot elongation in response to GA(3), and 58M showed GA(3)-mediated hastening of floral initiation when harvested at day 18 or 21. Both 90M and 100M had exhibited hastening of floral initiation by GA(3) previously, at later application dates. Tetcyclacis reduced height, promoted tillering, and delayed flowering of 58M resulting in plants which were near phenocopies of 90M and 100M. Based on bioassay activity, HPLC retention times, cochromatography with (2)H(2)-labeled standards on capillary column GC and matching mass spectrometer fragmentation patterns (ions [m/z] and relative abundances), GA(1), GA(19), GA(20), GA(53), and GA(3) were identified in extracts of all three genotypes. In addition, based on published Kovats retention index values and correspondence in ion masses and relative abundances, GA(44) and GA(17) were detected. Quantitation was based on recovery of coinjected, (2)H(2)-labeled standards. In 14 day-old-plants, total GA-like bioactivity and GA(1) concentrations (nanograms GA/gram dry weight) were two- to six-fold higher in 58M than 90M and 100M in leaf blades, apex samples, and whole plants while concentrations in culms were similar. Similar trends occurred if data were expressed on a per plant basis. GA(1) concentrations for whole plants were about two-fold higher in 58M than 90M and 100M from day 7 to day 14. Concentrations of ABA and IAA did not vary between the genotypes. The results indicate the mutant allele ma(3) (R) causes a two- to six-fold increase in GA(1) concentrations, does not result in a GA-receptor or transduction mutation and is associated with phenotypic characteristics that can be enhanced by GA(3) and reduced by GA synthesis inhibitor. These observations support the hypothesis that the allele ma(3) (R) causes an overproduction of GAs which results in altered leaf morphology, reduced tillering, earlier flowering, and other phenotypic differences between 58M and 90M or 100M.

Citing Articles

Fungal Diversity and Gibberellin Hormones Associated with Long Whips of Smut-Infected Sugarcanes.

Gillani S, Teng L, Khan A, Xu Y, Powell C, Zhang M Int J Mol Sci. 2024; 25(16).

PMID: 39201814 PMC: 11355029. DOI: 10.3390/ijms25169129.


High planting density induces the expression of GA3-oxidase in leaves and GA mediated stem elongation in bioenergy sorghum.

Yu K, McKinley B, Rooney W, Mullet J Sci Rep. 2021; 11(1):46.

PMID: 33420129 PMC: 7794234. DOI: 10.1038/s41598-020-79975-8.


Involvement of Auxin and Brassinosteroid in Dwarfism of Autotetraploid Apple (Malus × domestica).

Ma Y, Xue H, Zhang L, Zhang F, Ou C, Wang F Sci Rep. 2016; 6:26719.

PMID: 27216878 PMC: 4877651. DOI: 10.1038/srep26719.


Transcriptome Profiling of Tiller Buds Provides New Insights into PhyB Regulation of Tillering and Indeterminate Growth in Sorghum.

Kebrom T, Mullet J Plant Physiol. 2016; 170(4):2232-50.

PMID: 26893475 PMC: 4824614. DOI: 10.1104/pp.16.00014.


Plant growth enhancement and associated physiological responses are coregulated by ethylene and gibberellin in response to harpin protein Hpa1.

Li X, Han B, Xu M, Han L, Zhao Y, Liu Z Planta. 2014; 239(4):831-46.

PMID: 24395199 PMC: 3955481. DOI: 10.1007/s00425-013-2013-y.


References
1.
Rood S, Williams P, Pearce D, Murofushi N, Mander L, Pharis R . A mutant gene that increases gibberellin production in brassica. Plant Physiol. 1990; 93(3):1168-74. PMC: 1062647. DOI: 10.1104/pp.93.3.1168. View

2.
Bensen R, Beall F, Mullet J, Morgan P . Detection of endogenous gibberellins and their relationship to hypocotyl elongation in soybean seedlings. Plant Physiol. 1990; 94(1):77-84. PMC: 1077192. DOI: 10.1104/pp.94.1.77. View

3.
Koshioka M, Takeno K, Beall F, Pharis R . Purification and separation of plant gibberellins from their precursors and glucosyl conjugates. Plant Physiol. 1983; 73(2):398-406. PMC: 1066473. DOI: 10.1104/pp.73.2.398. View

4.
Fujioka S, Yamane H, Spray C, Gaskin P, MacMillan J, Phinney B . Qualitative and Quantitative Analyses of Gibberellins in Vegetative Shoots of Normal, dwarf-1, dwarf-2, dwarf-3, and dwarf-5 Seedlings of Zea mays L. Plant Physiol. 1988; 88(4):1367-72. PMC: 1055766. DOI: 10.1104/pp.88.4.1367. View

5.
Pao C, Morgan P . Genetic Regulation of Development in Sorghum bicolar: I. Role of the Maturity Genes. Plant Physiol. 1986; 82(2):575-80. PMC: 1056160. DOI: 10.1104/pp.82.2.575. View