New Phytologist最新文献

• Changes in chromosome numbers are a prominent driver of plant evolution, impacting ecological diversification, stress tolerance, and phenotypes. ChromEvol is a widely used software tool for deciphering patterns of chromosome-number change along a phylogeny of interest. It evaluates the fit of alternative models to the data, estimates transition rates of different types of events, and infers the expected number of events along each branch of the phylogeny.
• We introduce ChromEvol v.3, featuring multiple novel methodological advancements that capture variation in the transition rates along a phylogeny. This version better allows researchers to identify how dysploidy and polyploidy rates change based on the number of chromosomes in the genome, with respect to a discrete trait, or at certain subclades of the phylogeny.
• We demonstrate the applicability of the new models on the Solanaceae phylogeny. Our analyses identify four chromosome-number transition regimes that characterize distinct Solanaceae clades and demonstrate an association between self-compatibility and altered dynamics of chromosome-number evolution.
• ChromEvol v.3, available at https://github.com/anatshafir1/chromevol, offers researchers a more flexible, comprehensive, and accurate tool to investigate the evolution of chromosome numbers and the various processes affecting it.

• Abscisic acid (ABA) and jasmonic acid (JA) are important plant hormones in response to drought stress. We have identified that ZmHsf28 elevated ABA and JA accumulation to confer drought tolerance in maize; however, the underlying mechanism still remains elusive.
• The knockout line zmhsf28 is generated to confirm the positive role of ZmHsf28 in drought response. Multiple approaches are combined to reveal protein interaction among ZmHsf28, ZmSnRK2.2 and ZmJAZ14/17, which form a regulatory module to mediate maize drought tolerance through regulating ABA and JA key biosynthetic genes ZmNCED3 and ZmLOX8.
• Upon drought stress, zmhsf28 plants exhibit weaker tolerance than the WT plants with slower stomatal closure and more reactive oxygen species accumulation. ZmHsf28 interacted with ZmSnRK2.2 physically, resulting in phosphorylation at Ser220, which enhances binding to the heat shock elements of ZmNECD3 and ZmLOX8 promoters and subsequent gene expression. Meanwhile, ZmMYC2 upregulates ZmHsf28 gene expression through acting on the G-box of its promoter. Besides, ZmJAZ14/17 competitively interact with ZmHsf28 to interfere with protein interaction between ZmHsf28 and ZmSnRK2.2, blocking ZmHsf28 phosphorylation and impairing downstream gene regulation.
• The ZmSnRK2.2-ZmHsf28-ZmJAZ14/17 module is identified to regulate drought tolerance through coordinating ABA and JA signaling, providing the insights for breeding to improve drought resistance in maize.

• Plant height is a critical agronomic trait that affects crop yield, plant architecture, and environmental adaptability. Gibberellins (GAs) regulate plant height, with DELLA proteins acting as key repressors in the GA signaling pathway by inhibiting GA-induced growth. While DELLA phosphorylation is essential for regulating plant height, the precise mechanisms underlying this process remain incompletely understood.
• In this study, we identified a cucumber mutant with delayed growth, which exhibited reduced sensitivity to GA treatment. Through bulked segregant analysis (BSA-seq) combined with molecular marker linkage analysis, we successfully identified and cloned the gene responsible for the dwarf phenotype, CsIREH1 (INCOMPLETE ROOT HAIR ELONGATION 1), which encodes an AGC protein kinase.
• Further research revealed that CsIREH1 interacts with and phosphorylates DELLA proteins, specifically targeting CsGAIP and CsGAI2. We propose that IREH1-dependent phosphorylation of DELLA proteins prevents their excessive accumulation, thereby maintaining normal plant growth.
• Therefore, investigating the role of IREH1-mediated DELLA phosphorylation provides valuable insights and theoretical foundations for understanding how plants regulate growth mechanisms.

New Phytologist 244 (2024), 1408–1421, doi: 10.1111/nph.20153

Since its publication, the authors of El Arbi et al. (2024) have identified that under the heading ‘RNA extraction, strand-specific RNA sequencing and data analysis’, the text ‘MRNA sequences were aligned with Salmon (v.0.14.2) (Patro et al., 2017) to the A. thaliana Reference Transcript Dataset 2 (Zhang et al., 2017)’ should read ‘MRNA sequences were aligned with Salmon (v.0.14.2) (Patro et al., 2017) to the A. thaliana Reference Transcript Dataset 2 (AtRTD2-Quasi) (Zhang et al., 2017)’.

We apologise to our readers for this omission.

Author for correspondence:

Markus Schmid

Email: markus.schmid@slu.se

• There is an increasing demand to boost photosynthesis in rice to increase yield potential. Chloroplasts are the site of photosynthesis, and increasing their number and size is a potential route to elevate photosynthetic activity. Notably, bundle sheath cells do not make a significant contribution to overall carbon fixation in rice, and thus, various attempts are being made to increase chloroplast content specifically in this cell type.
• In this study, we developed and applied a deep learning tool, Chloro-Count, and used it to quantify chloroplast dimensions in bundle sheath cells of OsHAP3H gain- and loss-of-function mutants in rice.
• Loss of OsHAP3H increased chloroplast occupancy in bundle sheath cells by 50%. When grown in the field, mutants exhibited increased numbers of tillers and panicles. The implementation of Chloro-Count enabled precise quantification of chloroplasts in loss- and gain-of-function OsHAP3H mutants and facilitated a comparison between 2D and 3D quantification methods.
• Collectively, our observations revealed that a mechanism operates in bundle sheath cells to restrict chloroplast occupancy as cell dimensions increase. That mechanism is unperturbed in Oshap3H mutants but loss of OsHAP3H function leads to an increase in chloroplast numbers. The use of Chloro-Count also revealed that 2D quantification is compromised by the positioning of chloroplasts within the cell.

• Passion flower extrafloral nectaries (EFNs) protrude from leaves and facilitate mutualistic interactions with insects; however, how age cues control EFN growth remains poorly understood.
• Here, we examined leaf and EFN morphology and development of two Passiflora species with distinct leaf shapes, and compared the phenotype of these to transgenics with manipulated activity of the age-dependent miR156, which targets several SQUAMOSA PROMOTER-BINDING PROTEIN-LIKE (SPL) transcription factors.
• Low levels of miR156 correlated with leaf maturation and EFN formation in Passiflora edulis and P. cincinnata. Accordingly, manipulating miR156 activity affected leaf heteroblasty and EFN development. miR156-overexpressing leaves exhibited less abundant and tiny EFNs in both Passiflora species. EFN abundance remained mostly unchanged when miR156 activity was reduced, but it led to larger EFNs in P. cincinnata. Transcriptome analysis of young leaf primordia revealed that miR156-targeted SPLs may be required to properly express leaf and EFN-associated genes. Importantly, altered miR156 activity impacted sugar profiles of the nectar and modified ecological relationships between EFNs and ants.
• Our work provides evidence that the miR156/SPL module indirectly regulates EFN development in an age-dependent manner and that the EFN development program is closely associated with the heteroblastic developmental program of the EFN-bearing leaves.