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      Circadian Clock Genes Regulate Temperature-Dependent Diapause Induction in Silkworm Bombyx mori

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          Abstract

          The bivoltine strain of the domestic silkworm, Bombyx mori, exhibits a facultative diapause phenotype that is determined by maternal environmental conditions during embryonic and larval development. Although a recent study implicated a circadian clock gene period ( per) in circadian rhythms and photoperiod-induced diapause, the roles of other core feedback loop genes, including timeless ( tim), Clock ( Clk), cycle ( cyc), and cryptochrome2 ( cry2), have to be clarified yet. Therefore, the aim of this study was to elucidate the roles of circadian clock genes in temperature-dependent diapause induction. To achieve this, per, tim, Clk, cyc, and cry2 knockout (KO) mutants were generated, and the percentages of diapause and non-diapause eggs were determined. The results show that per, tim, Clk, cyc, and cry2 regulated temperature-induced diapause by acting upstream of cerebral γ-aminobutyric acid (GABA)ergic and diapause hormone signaling pathways. Moreover, the temporal expression of the clock genes in wild-type ( wt) silkworms was significantly different from that of thermosensitive transient receptor potential ankyrin 1 (TRPA1) KO mutants during embryonic development. Overall, the findings of this study provide target genes for regulating temperature-dependent diapause induction in silkworms.

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          Molecular mechanisms and physiological importance of circadian rhythms

          To accommodate daily recurring environmental changes, animals show cyclic variations in behaviour and physiology, which include prominent behavioural states such as sleep-wake cycles but also a host of less conspicuous oscillations in neurological, metabolic, endocrine, cardiovascular and immune functions. Circadian rhythmicity is created endogenously by genetically encoded molecular clocks, whose components cooperate to generate cyclic changes in their own abundance and activity, with a periodicity of about a day. Throughout the body, such molecular clocks convey temporal control to the function of organs and tissues by regulating pertinent downstream programmes. Synchrony between the different circadian oscillators and resonance with the solar day is largely enabled by a neural pacemaker, which is directly responsive to certain environmental cues and able to transmit internal time-of-day representations to the entire body. In this Review, we discuss aspects of the circadian clock in Drosophila melanogaster and mammals, including the components of these molecular oscillators, the function and mechanisms of action of central and peripheral clocks, their synchronization and their relevance to human health.
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            The monarch butterfly genome yields insights into long-distance migration.

            We present the draft 273 Mb genome of the migratory monarch butterfly (Danaus plexippus) and a set of 16,866 protein-coding genes. Orthology properties suggest that the Lepidoptera are the fastest evolving insect order yet examined. Compared to the silkmoth Bombyx mori, the monarch genome shares prominent similarity in orthology content, microsynteny, and protein family sizes. The monarch genome reveals a vertebrate-like opsin whose existence in insects is widespread; a full repertoire of molecular components for the monarch circadian clockwork; all members of the juvenile hormone biosynthetic pathway whose regulation shows unexpected sexual dimorphism; additional molecular signatures of oriented flight behavior; microRNAs that are differentially expressed between summer and migratory butterflies; monarch-specific expansions of chemoreceptors potentially important for long-distance migration; and a variant of the sodium/potassium pump that underlies a valuable chemical defense mechanism. The monarch genome enhances our ability to better understand the genetic and molecular basis of long-distance migration. Copyright © 2011 Elsevier Inc. All rights reserved.
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              GABA A receptor signalling mechanisms revealed by structural pharmacology

              Summary Type-A γ-aminobutyric receptors (GABAARs) are ligand-gated chloride channels with a very rich pharmacology. Some of their modulators, including benzodiazepines and general anaesthetics, are among the most successful drugs in clinical use and common substances of abuse. Without reliable structural data, the mechanistic basis for pharmacological modulation of GABAARs remains largely unknown. Here we report high-resolution cryoEM structures of the full-length human α1β3γ2L GABAAR in lipid nanodiscs, bound to the channel blocker picrotoxin, the competitive antagonist bicuculline, the agonist GABA and the classical benzodiazepines alprazolam (Xanax) and diazepam (Valium), respectively. We describe the binding modes and mechanistic impacts of these ligands, the closed and desensitised states of the GABAAR gating cycle, and the basis for allosteric coupling between the extracellular, agonist-binding, and the transmembrane, pore-forming, regions. This work provides a structural framework to integrate decades of physiology and pharmacology research and a rational basis for development of novel GABAAR modulators.
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                Author and article information

                Contributors
                Journal
                Front Physiol
                Front Physiol
                Front. Physiol.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                27 April 2022
                2022
                : 13
                : 863380
                Affiliations
                [1] 1 Faculty of Textile Science and Technology , Shinshu University , Ueda, Japan
                [2] 2 Graduate School of Science , Kyoto University , Kyoto, Japan
                [3] 3 Graduate School of Agriculture , Kyoto University , Kyoto, Japan
                [4] 4 Division of Liberal Arts and Sciences , Aichi Gakuin University , Nisshin, Japan
                Author notes

                Edited by: Jin-Jun Wang, Southwest University, China

                Reviewed by: Eran Tauber, University of Haifa, Israel

                Shi-Hong Gu, National Museum of Natural Science, Taiwan

                Ying Lin, Southwest University, China

                *Correspondence: Kunihiro Shiomi, shiomi@ 123456shinshu-u.ac.jp
                [ † ]

                These authors have contributed equally to this work

                This article was submitted to Invertebrate Physiology, a section of the journal Frontiers in Physiology

                Article
                863380
                10.3389/fphys.2022.863380
                9091332
                35574475
                3fc251c7-6285-4afb-a8f0-7a4915a50d28
                Copyright © 2022 Homma, Murata, Ikegami, Kobayashi, Yamazaki, Ikeda, Daimon, Numata, Mizoguchi and Shiomi.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 27 January 2022
                : 23 March 2022
                Categories
                Physiology
                Original Research

                Anatomy & Physiology
                clock gene,diapause,bombyx mori,transcription activator-like effector nuclease (talen),circadian clock

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