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The Orchidaceae is a large family of perennial herbs especially noted for the exceptional diversity of specialized flowers. Elucidating the genetic regulation of flowering and seed development of orchids is an important research goal with potential utility in orchid breeding programs. Auxin Response Factor (ARF) genes encode auxin-responsive transcription factors, which are involved in the regulation of diverse morphogenetic processes, including flowering and seed development. However, limited information on the ARF gene family in the Orchidaceae is available. In this study, 112 ARF genes were identified in the genomes of 5 orchid species (Apostasia shenzhenica, Dendrobium catenatum, Phalaenopsis aphrodite, Phalaenopsis equestris and Vanilla planifolia,). These genes were grouped into 7 subfamilies based on their phylogenetic relationships. Compared with the ARF family in model plants, such as Arabidopsis thaliana and Oryza sativa, one group of ARF genes involved in pollen wall synthesis has been lost during evolution of the Orchidaceae. This loss corresponds with absence of the exine in the pollinia. Through mining of the published genomic and transcriptomic data for the 5 orchid species: the ARF genes of subfamily 4 may play an important role in flower formation and plant growth, whereas those of subfamily 3 are potentially involved in pollen wall development. the study results provide novel insights into the genetic regulation of unique morphogenetic phenomena of orchids, which lay a foundation for further analysis of the regulatory mechanisms and functions of sexual reproduction-related genes in orchids.
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http://dx.doi.org/10.1007/s11103-023-01354-4 | DOI Listing |
Genes (Basel)
August 2025
Department of Biomedical Sciences, School of Biological and Environmental Sciences, Kwansei Gakuin University, 1 Gakuen Uegahara, Sanda 669-1330, Japan.
Background: DEAD/H box 5 (DDX5) serves as a transcriptional coactivator for several transcription factors including E2F1, the primary target of the tumor suppressor pRB. E2F1 physiologically activated by growth stimulation activates growth-related genes and promotes cell proliferation. In contrast, upon loss of pRB function due to oncogenic changes, E2F1 is activated out of restraint by pRB (deregulated E2F1) and stimulates tumor suppressor genes such as , which activates the tumor suppressor p53, to suppress tumorigenesis.
View Article and Find Full Text PDFBMC Genomics
August 2025
College of Horticulture, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Background: Chinese cherry [Cerasus pseudocerasus (Lindl.) G.Don], an economically important fruit species native to southwestern China, plays a key role in regional agriculture.
View Article and Find Full Text PDFBMC Plant Biol
August 2025
State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, Yunnan Agricultural University, Kunming, China.
Background: The invasive weed poses significant ecological threats, necessitating novel control strategies. This study investigated the phytotoxic potential of methyl indole-3-acetate (MEIAA) through foliar application. As a methylated derivative of IAA, MEIAA exists in plants at extremely low concentrations and exhibits herbicidal properties distinct from conventional auxin mimics such as 2,4-D.
View Article and Find Full Text PDFPlanta
August 2025
Henan International Joint Laboratory of Crop Gene Resource and Improvements, School of Agricultural Sciences, Zhengzhou University, Zhengzhou, 450001, China.
The rhizome bud development is governed by light signal, hormonal dynamics, carbohydrate metabolism, and cell cycle regulation in Arundo donax. Rhizomatous plants reproduce asexually through transplantation of rhizome segments bearing buds, which develop into new individuals. However, the regulatory mechanism governing rhizome bud differentiation and development is still unknown.
View Article and Find Full Text PDFNat Commun
August 2025
Department of Pediatrics, University of Rochester Medical Center, Rochester, NY, USA.
The limited proliferative capacity of erythroid precursors is a major obstacle to generate sufficient in vitro-derived red blood cells for clinical purposes. While BMI1, a Polycomb Repressive Complex 1 member, is both necessary and sufficient to drive extensive proliferation of self-renewing erythroblasts, its mechanism of action remains poorly understood. Here we report that BMI1 overexpression leads to 10 billion-fold increase in self-renewal of human erythroblasts, which can terminally mature and agglutinate with typing reagent monoclonal antibodies.
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