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Ben-Asher, H. W.

Publications and source records attributed to Ben-Asher, H. W..

2 recordsLinked to original sources

Disproportion of reticulon-like 16 (RTNLB16) splice variants expression disrupts growth and decreases sensitivity to ABA and senescence in Arabidopsis

The Reticulon family proteins (RTNs) are membrane-spanning proteins found in the endoplasmic reticulum (ER) with diverse functions, such as ER membrane morphogenesis, vesicle formation, and trafficking. The plant-specific reticulon-like protein family (RTNLBs) comprises multiple members, yet their functions remain poorly understood. The Arabidopsis RTNLB16 gene has seven splice variants, each encoding seven distinct protein isoforms. We identified an Arabidopsis mutant (Salk_122275/rtnlb16-1) as a knockout for the upper coding frame, isoform 7, of RTNLB16 while overexpressing the other six isoforms through the CaMV 35S promoter at the left border of the T-DNA insertion. rtnlb16-1 exhibits distinctive growth retardation and reduced chlorophyll levels. Under photoperiodic long day (16:8 h) conditions, activation of the 35S promoter intensifies RTNLB16 expression in the mutant, resulting in profound growth inhibition. Conversely, growth under continuous low-light (CLL) conditions restrains the overexpression and significantly mitigates rtnlb16-1 phenotype. Confocal microscopy experiments revealed the localization of RTNLB16:GFP in the tubular ER network, plasmodesmata, and potentially in Golgi bodies. Peculiarly, RTLB16/rtnlb16 heterozygote plants exhibit non-Mendelian reduced fertility, suggesting potential involvement of RTNLB16 in reproductive development. Transcriptomics comparisons between rtnlb16-1 and the wild type under CLL and 16:8h conditions revealed differential gene expression involved in salicylic acid, jasmonic acid, and abscisic acid responses, indicating activation of defense and osmotic stress responses contributing to the growth inhibition in the mutant. We further demonstrate that rtnlb16 has decreased sensitivity to abscisic acid and enhanced tolerance to darkness-induced senescence. Our findings highlight the importance of balanced expression among RTNLB16 isoforms for normal cellular and physiological activities in Arabidopsis. Additionally, our study underscores the significance of employing T-DNA mutants to investigate genes with multiple splice variants.

plant biology↗

Cyanobacterial sigma factor controls biofilm-promoting genes through intra- and intercellular pathways

Cyanobacteria frequently constitute integral components of microbial communities known as phototrophic biofilms. These assemblages are not only widespread in various environmental contexts but also hold significant industrial relevance. Nevertheless, the governing elements responsible for cyanobacterial biofilm development have remained elusive. This study, which employs the model cyanobacterium Synechococcus elongatus PCC 7942, demonstrates that the RNA polymerase sigma factor SigF1, but not its paralog SigF2, is required for a biofilm-suppression mechanism that operates in this organism. Comprehensive transcriptome analyses identified distinct regulons under the control of each of these sigma factors. Additional data indicate that SigF1 regulates biofilm through its involvement in transcriptional induction of genes that include those for the primary pilus subunit: sigF1 inactivation both prevents pilus assembly and abrogates secretion of a biofilm inhibitor. Consequently, expression is significantly upregulated for the ebfG-operon that encodes matrix components and the genes that encode their corresponding secretion system. Thus, this study uncovers a basic regulatory component of cyanobacterial communal behavior. Elevated expression of biofilm-promoting genes in a sigF1 mutant supports an additional layer of regulation by SigF1 that operates via an intracellular mechanism.

microbiology↗