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Cotton is a crucial fiber and oil crop, playing a significant role in the textile and food industries. Its yield heavily relies on photosynthesis, a process that primarily occurs in the leaves. Consequently, leaf morphology stands as a vital agronomic trait in cotton breeding. However, research on the molecular mechanisms underlying cotton leaf morphogenesis remains relatively limited. Here we identified a curly leaf mutant () in by ethyl methylsulfonate (EMS) mutagenesis. The genetic analysis revealed that the curly leaf trait in this mutant is a semi-dominant characteristic controlled by a single gene. The map-based cloning of the locus showed a single-nucleotide mutation from G to A at the 301st positions in protein (), which resulted in an amino acid substitution from valine (V) to isoleucine (I). After silencing through virus-induced gene silencing (VIGS) technology in mutant, the leaves exhibited a flattened phenotype, indicating that is a key gene regulating leaf curling in cotton. Comparative transcriptomic RNA-Seq analysis revealed significant changes in the expression levels of most auxin-related genes, suggesting that the mutation disrupts auxin signaling transduction. These findings establish a foundation for further functional studies of this gene and provide research strategies for leaf morphology improvement.
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http://dx.doi.org/10.3389/fpls.2025.1645239 | DOI Listing |
JCO Precis Oncol
September 2025
Cell Biology and Biotherapy Unit, Istituto Nazionale Tumori IRCCS Fondazione G. Pascale, Napoli, Italy.
Purpose: Tumor comprehensive genomic profiling (CGP) may detect potential germline pathogenic/likely pathogenic (P/LP) alterations as secondary findings. We analyzed the frequency of potentially germline variants and large rearrangements (LRs) in the RATIONAL study, an Italian multicenter, observational clinical trial that collects next-generation sequencing-based tumor profiling data, and evaluated how these findings were managed by the enrolling centers.
Patients And Methods: Patients prospectively enrolled in the pathway-B of the RATIONAL study and undergoing CGP with the FoundationOne CDx assays were included in the analysis.
Vet World
July 2025
Research Center for Applied Zoology, National Research and Innovation Agency, Republic of Indonesia, Bogor, Indonesia.
Background And Aim: The () gene plays a pivotal role in regulating growth, metabolism, and fat deposition in cattle. Genetic polymorphisms in this gene can influence phenotypic traits and may serve as molecular markers for selection in breeding programs. However, comprehensive characterization of gene variants in local Indonesian breeds, such as Madura cattle, remains limited.
View Article and Find Full Text PDFBackground: A significant surge in pertussis cases since early 2023 has raised serious public health concerns. To investigate the potential mechanisms contributing to this increased prevalence, we collected throat swab specimens from children exhibiting pertussis symptoms and conducted detailed molecular characterization.
Methods: All Bordetella pertussis (B.
Medicine (Baltimore)
September 2025
Department of Pediatrics, Affiliated Hospital of Jining Medical University, Jining, Shandong Province, China.
Rationale: Weaver syndrome is a rare congenital overgrowth disorder characterized by a wide spectrum of clinical manifestations that often overlap with other overgrowth syndromes. It is primarily caused by pathogenic variants in the Enhancer of Zeste Homolog 2 (EZH2) gene on chromosome 7q36.1.
View Article and Find Full Text PDFPLoS One
September 2025
Department of Pharmacy, Faculty of Science, Noakhali Science and Technology University, Sonapur, Bangladesh.
Background: Overexpression of rs3761936 of DCLRE1B gene has been observed in both breast cancer and cervical cancer patients. To justify the association of this polymorphism with these cancers, we performed this case-control study.
Method: A total of 245 cancer patients and 108 healthy controls participated in the research.