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      A leak K + channel TWK-40 sustains the rhythmic motor program

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          Abstract

          Leak potassium (K +) currents, conducted by two-pore domain K + (K 2P) channels, are critical for the stabilization of the membrane potential. The effect of K 2P channels on motor rhythm remains enigmatic. We show here that the K 2P TWK-40 contributes to the rhythmic defecation motor program (DMP) in Caenorhabditis elegans. Disrupting TWK-40 suppresses the expulsion defects of nlp-40 and aex-2 mutants. By contrast, a gain-of-function ( gf) mutant of twk-40 significantly reduces the expulsion frequency per DMP cycle. In situ whole-cell patch clamping demonstrates that TWK-40 forms an outward current that hyperpolarize the resting membrane potential of dorsorectal ganglion ventral process B (DVB), an excitatory GABAergic motor neuron that activates expulsion muscle contraction. In addition, TWK-40 substantially contributes to the rhythmic activity of DVB. Specifically, DVB Ca 2+ oscillations exhibit obvious defects in loss-of-function ( lf) mutant of twk-40. Expression of TWK-40( gf) in DVB recapitulates the expulsion deficiency of the twk-40(gf) mutant, and inhibits DVB Ca 2+ oscillations in both wild-type and twk-40(lf) animals. Moreover, DVB innervated enteric muscles also exhibit rhythmic Ca 2+ defects in twk-40 mutants. In summary, these findings establish TWK-40 as a crucial neuronal stabilizer of DMP, linking leak K 2P channels with rhythmic motor activity.

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          Most cited references54

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          The Structure of the Nervous System of the Nematode Caenorhabditis elegans

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            Molecular background of leak K+ currents: two-pore domain potassium channels.

            Two-pore domain K(+) (K(2P)) channels give rise to leak (also called background) K(+) currents. The well-known role of background K(+) currents is to stabilize the negative resting membrane potential and counterbalance depolarization. However, it has become apparent in the past decade (during the detailed examination of the cloned and corresponding native K(2P) channel types) that this primary hyperpolarizing action is not performed passively. The K(2P) channels are regulated by a wide variety of voltage-independent factors. Basic physicochemical parameters (e.g., pH, temperature, membrane stretch) and also several intracellular signaling pathways substantially and specifically modulate the different members of the six K(2P) channel subfamilies (TWIK, TREK, TASK, TALK, THIK, and TRESK). The deep implication in diverse physiological processes, the circumscribed expression pattern of the different channels, and the interesting pharmacological profile brought the K(2P) channel family into the spotlight. In this review, we focus on the physiological roles of K(2P) channels in the most extensively investigated cell types, with special emphasis on the molecular mechanisms of channel regulation.
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              Whole-animal connectomes of both Caenorhabditis elegans sexes

              Knowledge of connectivity in the nervous system is essential to understanding its function. Here we describe connectomes for both adult sexes of the nematode Caenorhabditis elegans, an important model organism for neuroscience research. We present quantitative connectivity matrices that encompass all connections from sensory input to end-organ output across the entire animal, information that is necessary to model behaviour. Serial electron microscopy reconstructions that are based on the analysis of both new and previously published electron micrographs update previous results and include data on the male head. The nervous system differs between sexes at multiple levels. Several sex-shared neurons that function in circuits for sexual behaviour are sexually dimorphic in structure and connectivity. Inputs from sex-specific circuitry to central circuitry reveal points at which sexual and non-sexual pathways converge. In sex-shared central pathways, a substantial number of connections differ in strength between the sexes. Quantitative connectomes that include all connections serve as the basis for understanding how complex, adaptive behavior is generated.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PNAS Nexus
                PNAS Nexus
                pnasnexus
                PNAS Nexus
                Oxford University Press (US )
                2752-6542
                July 2024
                12 June 2024
                12 June 2024
                : 3
                : 7
                : pgae234
                Affiliations
                Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology , Wuhan 430074, China
                Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology , Wuhan 430074, China
                Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology , Wuhan 430074, China
                College of Biomedical Engineering, South-Central University for Nationalities , Wuhan 430074, China
                Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology , Wuhan 430074, China
                Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto , Toronto, ON M5G 1X5, Canada
                Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto , Toronto, ON M5G 1X5, Canada
                Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto , Toronto, ON M5G 1X5, Canada
                Department of Geriatrics, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, China
                Univ Lyon, Université Claude Bernard Lyon 1, MeLiS, CNRS UMR 5284, INSERM U1314, Institut NeuroMyoGène , Lyon 69008, France
                King Abdullah University of Science and Technology (KAUST), Biological and Environmental Sciences and Engineering Division (BESE) , Thuwal 23955–6900, Kingdom of Saudi Arabia
                Department of Geriatrics, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, China
                Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto , Toronto, ON M5G 1X5, Canada
                Univ Lyon, Université Claude Bernard Lyon 1, MeLiS, CNRS UMR 5284, INSERM U1314, Institut NeuroMyoGène , Lyon 69008, France
                Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology , Wuhan 430074, China
                Department of Geriatrics, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, China
                Author notes
                To whom correspondence should be addressed: Email: sgao@ 123456hust.edu.cn

                Z.Y., Y.L., B.Y., and Y.X. contributed equally to this work.

                Competing Interest: The authors declare no competing interest.

                Author information
                https://orcid.org/0000-0002-3719-7631
                https://orcid.org/0000-0002-2907-2169
                https://orcid.org/0000-0002-4165-8496
                https://orcid.org/0000-0002-3674-3151
                https://orcid.org/0000-0002-2365-5646
                https://orcid.org/0000-0002-1734-1915
                https://orcid.org/0000-0001-5431-4628
                Article
                pgae234
                10.1093/pnasnexus/pgae234
                11217676
                38957449
                9aaea5be-f98c-4797-ad4f-19770c4beec3
                © The Author(s) 2024. Published by Oxford University Press on behalf of National Academy of Sciences.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence ( https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

                History
                : 19 February 2024
                : 05 June 2024
                : 02 July 2024
                Page count
                Pages: 11
                Funding
                Funded by: Major International (Regional) Joint Research Project;
                Award ID: 32020103007
                Funded by: National Natural Science Foundation of China, DOI 10.13039/501100001809;
                Award ID: 32371189
                Award ID: 31871069
                Funded by: National Key Research and Development Program of China, DOI 10.13039/501100012166;
                Award ID: 2022YFA1206001
                Funded by: Overseas High-level Talents Introduction Program;
                Funded by: European Research Council, DOI 10.13039/100010663;
                Categories
                Biological, Health, and Medical Sciences
                AcademicSubjects/MED00010
                AcademicSubjects/SCI00010
                AcademicSubjects/SOC00010
                PNAS_Nexus/neuro

                twk-40,k2p channel,motor rhythm,ca2+ oscillation,membrane potential

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