Four monogenic, recessive dwarf mutants of lettuce (Lactuca sativa L.), previously isolated from a population induced by ethyl methanesulfonate, were compared with the normal genotype (E-1) for plant height, weight, leaf area, as well as hypocotyl length and root length. These nonallelic dwarfs (dwf1, dwf2, and dwf3) exhibited reduced hypocotyl length, smaller, dark green leaves, and reduced stem length. Another mutant, dwf2, allelic with dwf2, exhibited an intermediate phenotype. Epidermal cells on hypocotyls and mature leaves were counted for both normal E-1 and dwf2 plants. The total number of epidermal cells per unit area for hypocotyls and for leaves from these plants was very similar, implying the dwarf's smaller size was due to an inhibition of cell expansion and not due to decreased cell divisions. Both dwarf and normal hypocotyls elongated normally in response to exogenous gibberellin A(3) (GA(3)). In the rosette stage, only E-1 and dwf2 responded similarly to lower concentrations of GA(3), while the other dwarfs required higher concentrations to respond. Hypocotyls of dwf2 and E-1 elongated equally with applied ent-kaurenol, ent-kaurenoic acid, GA(53)-aldehyde, GA(53), GA(19), GA(20), and GA(1) indicating that the biochemical block in dwf2 occurs at a very early step in the GA-biosynthetic pathway.
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http://dx.doi.org/10.1104/pp.95.4.1162 | DOI Listing |
Int J Mol Sci
December 2024
Department of Pediatrics, McGovern Medical School UTHealth, Houston, TX 77030, USA.
Pseudoachondroplasia (PSACH), a severe dwarfing condition characterized by impaired skeletal growth and early joint degeneration, results from mutations in cartilage oligomeric matrix protein (COMP). These mutations disrupt normal protein folding, leading to the accumulation of misfolded COMP in chondrocytes. The MT-COMP mouse is a murine model of PSACH that expresses D469del human COMP in response to doxycycline and replicates the PSACH chondrocyte and clinical pathology.
View Article and Find Full Text PDFJ Plant Physiol
January 2025
State Key Laboratory of Crop Gene Resources and Breeding/National Engineering Laboratory of Crop Molecular Breeding/CAEA Research and Development Centre on Nuclear Technology Applications for Irradiation Mutation Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China. Electronic address:
Plant height determines lodging resistance and is closely linked to yield stability in wheat. In this study, we identified two semi-dwarf wheat mutants, designated je0370 and je0344, using the winter wheat cultivar Jing411 as the wild type (WT). Field experiments revealed that the plant height of these two mutants was significantly lower than that of the WT.
View Article and Find Full Text PDFGenes (Basel)
December 2024
Henan Technology Innovation Centre of Wheat/National Engineering Research Centre for Wheat, Henan Agricultural University, Zhengzhou 450046, China.
Background: The tiller number is a key agronomic trait for increasing the yield potential of wheat ( L.). A number of quantitative trait loci (QTLs) and key genes controlling tillering have been identified, but the regulatory mechanisms remain unclear.
View Article and Find Full Text PDFPlant Physiol
January 2025
Institute of Biology, Biotechnology and Environmental Protection, Faculty of Natural Sciences, University of Silesia, Katowice, Poland.
Global climate change leads to the increased occurrence of environmental stress (including drought and heat stress) during the vegetative and reproductive stages of cereal crop development. Thus, more attention should be given to developing new cereal cultivars with improved tolerance to environmental stress. However, during the development of new stress-tolerant cereal cultivars, the balance between improved stress responses (which occur at the expense of growth) and plant yield needs to be maintained.
View Article and Find Full Text PDFFront Endocrinol (Lausanne)
January 2025
Departamento de Bioquímica Clínica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Córdoba, Argentina.
Introduction: The sodium/iodide symporter (NIS) mediates active iodide accumulation in the thyroid follicular cell. Biallelic loss-of-function variants in the NIS-coding gene cause congenital dyshormonogenic hypothyroidism due to a defect in the accumulation of iodide, which is required for thyroid hormonogenesis.
Objective: We aimed to identify, and if so to functionally characterize, novel pathogenic gene variants in a patient diagnosed with severe congenital dyshormonogenic hypothyroidism characterized by undetectable radioiodide accumulation in a eutopic thyroid gland, as well as in the salivary glands.
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