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Temperature is a major factor regulating plant growth. To reproduce at extreme temperatures, plants must develop normal reproductive organs when exposed to temperature changes. However, little is known about the underlying molecular mechanisms. Here, we identified the maize () mutant - (-), which lacks tassels at high (restrictive) temperatures due to shoot apical meristem (SAM) arrest, but forms normal tassels at moderate (permissive) temperatures. The critical stage for phenotypic conversion in - mutants is V2 to V6 (Vn, where "n" is the number of leaves with collars visible). Positional cloning and allelism and complementation tests revealed that a G-to-A mutation causing a Arg-to-His substitution in ZmRNRL1, a ribonucleotide reductase (RNR) large subunit (RNRL), confers the - mutant phenotype. RNR regulates the rate of deoxyribonucleoside triphosphate (dNTP) production for DNA replication and damage repair. By expression, yeast two-hybrid, RNA sequencing, and flow cytometric analyses, we found that ZmRNRL1-- failed to interact with all three RNR small subunits at 34°C due to the Arg-to-His substitution, which could impede RNR holoenzyme (αβ) formation, thereby decreasing the dNTP supply for DNA replication. Decreased dNTP supply may be especially severe for the SAM that requires a continuous, sufficient dNTP supply for rapid division, as demonstrated by the SAM arrest and tassel absence in - mutants at restrictive temperatures. Our study reveals a novel mechanism of temperature-gated tassel formation in maize and provides insight into the role of RNRL in SAM maintenance.
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http://dx.doi.org/10.1104/pp.20.00219 | DOI Listing |
Ann Card Anaesth
July 2025
Department of Anaesthesiology, Institute of Medicine (IOM), Tribhuvan University Teaching Hospital(TUTH), Nepal.
Introduction: Invasive blood pressure monitoring is the clinical reference during perioperative patient management. It is usually performed by cannulating the radial artery. Different clinical conditions make arterial cannulation difficult using the conventional palpation (CP) method.
View Article and Find Full Text PDFFront Microbiol
April 2025
Department of Science and Environment, Roskilde University, Roskilde, Denmark.
Replication fork speed (RFS) in has long been considered constant throughout the replication and cell cycles. In wild-type cells, the circular chromosome is duplicated bidirectionally from , yielding two replication forks that converge at the ter region. Under slow-growth conditions, cells are smaller at initiation than at termination, so DNA replication consumes a larger fraction of cellular resources early in the cell cycle.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
April 2025
Department of Medical Biochemistry and Biophysics, Umeå University, Umeå SE 90187, Sweden.
Mitochondrial DNA (mtDNA) replication requires a steady supply of deoxyribonucleotides (dNTPs), synthesized de novo by ribonucleotide reductase (RNR). In nondividing cells, RNR consists of RRM1 and RRM2B subunits. Mutations in cause mtDNA depletion syndrome, linked to muscle weakness, neurological decline, and early mortality.
View Article and Find Full Text PDFMol Ther Nucleic Acids
June 2025
State Key Laboratory of Reproductive Medicine and Offspring Health, Center for Reproductive Medicine, Institute of Women, Children and Reproductive Health, Shandong University, Jinan, Shandong 250012, China.
Assisted reproductive technology (ART) is used widely and efficiently to treat infertility. During the ART procedure, one of the main factors affecting the success rate is abnormal development of preimplantation embryos. The establishment and maintenance of developmental competence are precisely regulated at different levels, while minor errors at early stages may result in adverse outcomes, including developmental arrest and implantation failure.
View Article and Find Full Text PDFBiotechnol Bioeng
December 2024
Chemical Engineering and Biotechnology, University of Cambridge, Cambridge, UK.
Low availability of routine nucleic acid amplification testing (NAAT) during infection outbreaks, especially in less resourced environments, was highlighted by the Covid pandemic. One of the barriers lies with the supply chain and cost of the active diagnostic ingredients (ADIs) that are the reagents for NAATs. This work explores a novel synthesis method to produce a key NAAT reagent, namely the 2'-deoxynucleoside 5'-triphosphate (dNTPs), via a reusable enzyme bioreactor, that can be integrated into a NAAT workflow.
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