The Saccharomyces cerevisiae SHC1 gene encodes a protein with a high homology to Chs4p, a positive regulator of chitin synthase III (CSIII) during vegetative growth. SHC1 is not expressed during vegetative growth but is strongly induced during sporulation as a mid-late gene. shc1/shc1 mutants do not show any defect in the total rate of sporulation and meiosis occurs normally. However, shc1/shc1 ascospores be-come highly permeable to DAPI, much more sensitive to glusulase treatment, and have very low levels of chitosan in their cell walls. All these observations indicate that Shc1p is required for proper maturation of the ascospore through its participation in the synthesis of the chitosan layer. Lack of SHC1 during sporulation can be partially compensated by over-expression of the CHS4 gene. During vegetative growth, SHC1 has no apparent function but, when ectopically overexpressed, it can substitute Chs4p as an activator of the CSIII activity; however, Shc1p fails to localize it properly, as Chs4p does. In conclusion, S. cerevisiae contains two functionally redundant genes in the control of CSIII activity: CHS4, whose function is restricted to vegetative growth because Chs4p is rapidly degraded during sporulation, and SHC1, whose function in cell wall ascospore assembly is transcriptionally restricted to the sporulation process.
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http://dx.doi.org/10.1046/j.1365-2958.2002.02812.x | DOI Listing |
Sci Total Environ
January 2025
Department for Sustainable Food Process, Università Cattolica del Sacro Cuore, 29122 Piacenza, Italy. Electronic address:
Polyethylene nanoplastics (NPs) are widely diffused in terrestrial environments, including soil ecosystems, but the stress mechanisms in plants are not well understood. This study aimed to investigate the effects of two increasing concentrations of NPs (20 and 200 mg kg of soil) in lettuce. To this aim, high-throughput hyperspectral imaging was combined with metabolomics, covering both primary (using NMR) and secondary metabolism (using LC-HRMS), along with lipidomics profiling (using ion-mobility-LC-HRMS) and plant performance.
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Department of Applied Biological Science, Faculty of Agriculture, Kagawa University, Miki, Kita 761-0795, Kagawa, Japan.
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Department of Plant and Soil Sciences, Faculty of Agriculture, Chiang Mai University, Chiang Mai 50200, Thailand.
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January 2025
Department of Genomics and Evolutionary Biology, National Institute of Genetics, Mishima 411-8540, Japan.
During vegetative growth, plants undergo various morphological and physiological changes in the transition from the juvenile phase to the adult phase. In terms of stress resistance, it has been suggested that plants gain or reinforce disease resistance during the process of maturation, which is recognized as adult plant resistance or age-related resistance. While much knowledge has been obtained about changes in disease resistance as growth stages progress, knowledge about changes in plant responses to pathogens with progressing age in plants is limited.
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College of Forestry, Northeast Forestry University, Harbin 150040, China.
The utilization of nitrogen (N) is crucial for the optimal growth and development of plants. As the dominant form of nitrogen in temperate soil, nitrate (NO) is absorbed from the soil and redistributed to other organs through NO transporters (NRTs). Therefore, exploration of the role of NRTs in response to various NO conditions is crucial for improving N utilization efficiency (NUE).
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