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  1. Article: Development of novel tools for dissection of central versus peripheral dopamine D

    Bonifazi, Alessandro / Ellenberger, Michael / Farino, Zachary J / Aslanoglou, Despoina / Rais, Rana / Pereira, Sandra / Mantilla-Rivas, José O / Boateng, Comfort A / Eshleman, Amy J / Janowsky, Aaron / Hahn, Margaret K / Schwartz, Gary J / Slusher, Barbara S / Newman, Amy Hauck / Freyberg, Zachary

    bioRxiv : the preprint server for biology

    2024  

    Abstract: Dopamine (DA) D ...

    Abstract Dopamine (DA) D
    Language English
    Publishing date 2024-02-24
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2024.02.21.581451
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Precise Measurement of the D_{s}^{+} Lifetime at Belle II.

    Adachi, I / Aggarwal, L / Aihara, H / Akopov, N / Aloisio, A / Anh Ky, N / Asner, D M / Atmacan, H / Aushev, T / Aushev, V / Aversano, M / Babu, V / Bae, H / Bahinipati, S / Bambade, P / Banerjee, Sw / Barrett, M / Baudot, J / Bauer, M /
    Baur, A / Beaubien, A / Becker, J / Behera, P K / Bennett, J V / Bernlochner, F U / Bertacchi, V / Bertemes, M / Bertholet, E / Bessner, M / Bettarini, S / Bhuyan, B / Bianchi, F / Bilka, T / Biswas, D / Bodrov, D / Bondar, A / Bozek, A / Bračko, M / Branchini, P / Briere, R A / Browder, T E / Budano, A / Bussino, S / Campajola, M / Cao, L / Casarosa, G / Cecchi, C / Cerasoli, J / Chang, M-C / Chang, P / Cheema, P / Chekelian, V / Cheon, B G / Chilikin, K / Chirapatpimol, K / Cho, H-E / Cho, K / Choi, S-K / Choudhury, S / Cochran, J / Corona, L / Das, S / Dattola, F / De La Motte, S A / de Marino, G / De Nardo, G / De Nuccio, M / De Pietro, G / de Sangro, R / Destefanis, M / Dey, S / Dhamija, R / Di Canto, A / Di Capua, F / Dingfelder, J / Doležal, Z / Domínguez Jiménez, I / Dong, T V / Dorigo, M / Dort, K / Dreyer, S / Dubey, S / Dujany, G / Ecker, P / Epifanov, D / Feichtinger, P / Ferlewicz, D / Finck, C / Finocchiaro, G / Fodor, A / Forti, F / Frey, A / Fulsom, B G / Gabrielli, A / Ganiev, E / Garcia-Hernandez, M / Garmash, A / Gaudino, G / Gaur, V / Gaz, A / Gellrich, A / Ghevondyan, G / Ghosh, D / Ghumaryan, H / Giakoustidis, G / Giordano, R / Giri, A / Glazov, A / Gobbo, B / Godang, R / Gogota, O / Goldenzweig, P / Gradl, W / Graziani, E / Greenwald, D / Gruberová, Z / Gu, T / Guan, Y / Gudkova, K / Han, Y / Hayasaka, K / Hayashii, H / Hazra, S / Hearty, C / Heredia de la Cruz, I / Hershenhorn, A / Higuchi, T / Hill, E C / Hoek, M / Hohmann, M / Hsu, C-L / Humair, T / Iijima, T / Inami, K / Ipsita, N / Ishikawa, A / Ito, S / Itoh, R / Iwasaki, M / Jackson, P / Jacobs, W W / Jaffe, D E / Jang, E-J / Ji, Q P / Jia, S / Jin, Y / Junkerkalefeld, H / Kaliyar, A B / Kandra, J / Karyan, G / Kawasaki, T / Keil, F / Ketter, C / Kiesling, C / Kim, C-H / Kim, D Y / Kim, K-H / Kim, Y-K / Kindo, H / Kinoshita, K / Kodyš, P / Koga, T / Kohani, S / Kojima, K / Korobov, A / Korpar, S / Kowalewski, R / Kraetzschmar, T M G / Križan, P / Krokovny, P / Kuhr, T / Kumar, J / Kumar, M / Kumar, R / Kumara, K / Kuzmin, A / Kwon, Y-J / Lacaprara, S / Lai, Y-T / Lam, T / Lange, J S / Laurenza, M / Leboucher, R / Le Diberder, F R / Leitl, P / Levit, D / Lewis, P M / Li, L K / Libby, J / Liu, Q Y / Liu, Z Q / Liventsev, D / Longo, S / Lueck, T / Lyu, C / Ma, Y / Maggiora, M / Maharana, S P / Maiti, R / Maity, S / Manfredi, R / Manoni, E / Mantovano, M / Marcantonio, D / Marcello, S / Marinas, C / Martellini, C / Martini, A / Martinov, T / Massaccesi, L / Masuda, M / Matsuda, T / Matsuoka, K / Matvienko, D / Maurya, S K / McKenna, J A / Mehta, R / Meier, F / Merola, M / Metzner, F / Milesi, M / Miller, C / Mirra, M / Miyabayashi, K / Mohanty, G B / Molina-Gonzalez, N / Mondal, S / Moneta, S / Moser, H-G / Mrvar, M / Mussa, R / Nakamura, I / Nakazawa, Y / Narimani Charan, A / Naruki, M / Natkaniec, Z / Natochii, A / Nayak, L / Nazaryan, G / Nisar, N K / Nishida, S / Ono, H / Otani, F / Oxford, E R / Pakhlov, P / Pakhlova, G / Paladino, A / Panta, A / Paoloni, E / Pardi, S / Passeri, A / Patra, S / Paul, S / Pedlar, T K / Peruzzi, I / Peschke, R / Pestotnik, R / Pham, F / Piccolo, M / Piilonen, L E / Podobnik, T / Pokharel, S / Praz, C / Prell, S / Prencipe, E / Prim, M T / Purwar, H / Rados, P / Raeuber, G / Raiz, S / Reif, M / Reiter, S / Remnev, M / Ripp-Baudot, I / Rizzo, G / Roney, J M / Rostomyan, A / Rout, N / Russo, G / Sandilya, S / Sangal, A / Santelj, L / Sato, Y / Savinov, V / Scavino, B / Schmitt, C / Schwanda, C / Schwartz, A J / Seino, Y / Selce, A / Senyo, K / Serrano, J / Sevior, M E / Sfienti, C / Shan, W / Shi, X D / Shillington, T / Shiu, J-G / Shtol, D / Sibidanov, A / Simon, F / Sobie, R J / Sobotzik, M / Soffer, A / Sokolov, A / Solovieva, E / Spataro, S / Spruck, B / Starič, M / Stavroulakis, P / Stottler, Z S / Stroili, R / Sumihama, M / Svidras, H / Takahashi, M / Takizawa, M / Tamponi, U / Tanida, K / Tenchini, F / Tittel, O / Tonelli, D / Torassa, E / Trabelsi, K / Tsaklidis, I / Unger, K / Unno, Y / Uno, K / Uno, S / Urquijo, P / Ushiroda, Y / Vahsen, S E / van Tonder, R / Varvell, K E / Veronesi, M / Vismaya, V S / Vitale, L / Volpe, R / Wach, B / Wallner, S / Wang, E / Wang, M-Z / Wang, X L / Wang, Z / Warburton, A / Watanabe, M / Wessel, C / Won, E / Xu, X P / Yabsley, B D / Yamada, S / Yan, W / Yang, S B / Yoshihara, K / Yuan, C Z / Yusa, Y / Zhang, Y / Zhilich, V / Zhou, J S / Zhou, Q D / Zhukova, V I / Žlebčík, R

    Physical review letters

    2023  Volume 131, Issue 17, Page(s) 171803

    Abstract: We measure the lifetime of the D_{s}^{+} meson using a data sample of 207  fb^{-1} collected ... determined by fitting the decay-time distribution of a sample of 116×10^{3} D_{s}^{+}→ϕπ^{+} decays ... Our result is τ_{D_{s}^{+}}=(499.5±1.7±0.9)  fs, where the first uncertainty is statistical and the second is ...

    Abstract We measure the lifetime of the D_{s}^{+} meson using a data sample of 207  fb^{-1} collected by the Belle II experiment running at the SuperKEKB asymmetric-energy e^{+}e^{-} collider. The lifetime is determined by fitting the decay-time distribution of a sample of 116×10^{3} D_{s}^{+}→ϕπ^{+} decays. Our result is τ_{D_{s}^{+}}=(499.5±1.7±0.9)  fs, where the first uncertainty is statistical and the second is systematic. This result is significantly more precise than previous measurements.
    Language English
    Publishing date 2023-11-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 208853-8
    ISSN 1079-7114 ; 0031-9007
    ISSN (online) 1079-7114
    ISSN 0031-9007
    DOI 10.1103/PhysRevLett.131.171803
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  3. Article ; Online: 1α,25-Dihydroxyvitamin D

    Asmussen, Niels C / Alam, Sheikh / Lin, Zhao / Cohen, David J / Schwartz, Zvi / Boyan, Barbara D

    Calcified tissue international

    2023  Volume 112, Issue 4, Page(s) 493–511

    Abstract: ... and export matrix vesicles (MVs) under the regulation of 1α,25-dihydroxyvitamin D ...

    Abstract Growth plate chondrocytes are regulated by numerous factors and hormones as they mature during endochondral bone formation, including transforming growth factor beta-1 (TGFb1), bone morphogenetic protein 2 (BMP2), insulin-like growth factor-1 (IFG1), parathyroid hormone and parathyroid hormone related peptide (PTH, PTHrP), and Indian hedgehog (IHH). Chondrocytes in the growth plate's growth zone (GC) produce and export matrix vesicles (MVs) under the regulation of 1α,25-dihydroxyvitamin D
    MeSH term(s) MicroRNAs/metabolism ; Hedgehog Proteins/metabolism ; Chondrocytes/metabolism ; Extracellular Matrix/metabolism ; Cells, Cultured
    Chemical Substances 1,25-dihydroxyvitamin D (66772-14-3) ; MicroRNAs ; Hedgehog Proteins
    Language English
    Publishing date 2023-02-25
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 304266-2
    ISSN 1432-0827 ; 0944-0747 ; 0008-0594 ; 0171-967X
    ISSN (online) 1432-0827
    ISSN 0944-0747 ; 0008-0594 ; 0171-967X
    DOI 10.1007/s00223-023-01067-2
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  4. Article ; Online: 24R,25-dihydroxyvitamin D

    Verma, Anjali / Schwartz, Zvi / Boyan, Barbara D

    Steroids

    2019  Volume 150, Page(s) 108447

    Abstract: Vitamin D has long been prescribed as a supplement to breast cancer patients. This is partially ... motivated by data indicating that low serum vitamin D, measured as 25-hydroxyvitamin D3 [25(OH)D ...

    Abstract Vitamin D has long been prescribed as a supplement to breast cancer patients. This is partially motivated by data indicating that low serum vitamin D, measured as 25-hydroxyvitamin D3 [25(OH)D
    MeSH term(s) 24,25-Dihydroxyvitamin D 3/metabolism ; 24,25-Dihydroxyvitamin D 3/pharmacology ; Animals ; Breast Neoplasms/diet therapy ; Breast Neoplasms/metabolism ; Breast Neoplasms/pathology ; Female ; Humans ; Mammary Neoplasms, Experimental/diet therapy ; Mammary Neoplasms, Experimental/metabolism ; Mammary Neoplasms, Experimental/pathology ; Receptors, Estrogen/metabolism
    Chemical Substances Receptors, Estrogen ; 24,25-Dihydroxyvitamin D 3 (40013-87-4)
    Language English
    Publishing date 2019-07-11
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 80312-1
    ISSN 1878-5867 ; 0039-128X
    ISSN (online) 1878-5867
    ISSN 0039-128X
    DOI 10.1016/j.steroids.2019.108447
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  5. Article ; Online: 24R,25-Dihydroxyvitamin D

    Verma, Anjali / Cohen, D Joshua / Schwartz, Nofrat / Muktipaty, Chandana / Koblinski, Jennifer E / Boyan, Barbara D / Schwartz, Zvi

    Biochimica et biophysica acta. General subjects

    2019  Volume 1863, Issue 10, Page(s) 1498–1512

    Abstract: Background: Epidemiological studies indicate high serum 25(OH)D: Methods: NOD-SCID-IL2γR null ...

    Abstract Background: Epidemiological studies indicate high serum 25(OH)D
    Methods: NOD-SCID-IL2γR null female mice with MCF7 breast cancer xenografts in the mammary fat pad were treated with 24R,25(OH)
    Results: 24R,25(OH)
    Conclusion: These results indicate that 24R,25(OH)
    General significance: 24R,25(OH)
    MeSH term(s) 24,25-Dihydroxyvitamin D 3/metabolism ; Animals ; Breast Neoplasms/metabolism ; Breast Neoplasms/pathology ; Cell Proliferation/drug effects ; Estradiol/administration & dosage ; Estradiol/pharmacology ; Female ; Humans ; MCF-7 Cells ; Mice ; Mice, Inbred NOD ; Phospholipase D/metabolism ; Receptors, Estrogen/metabolism ; Signal Transduction
    Chemical Substances Receptors, Estrogen ; 24,25-Dihydroxyvitamin D 3 (40013-87-4) ; Estradiol (4TI98Z838E) ; Phospholipase D (EC 3.1.4.4)
    Language English
    Publishing date 2019-05-22
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 60-7
    ISSN 1872-8006 ; 1879-2596 ; 1879-260X ; 1879-2642 ; 1879-2618 ; 1879-2650 ; 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    ISSN (online) 1872-8006 ; 1879-2596 ; 1879-260X ; 1879-2642 ; 1879-2618 ; 1879-2650
    ISSN 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    DOI 10.1016/j.bbagen.2019.05.013
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  6. Article ; Online: Local production of active vitamin D

    Dennis, Cydney / Dillon, Jonathan / Cohen, David J / Halquist, Matthew S / Pearcy, Adam C / Schwartz, Zvi / Boyan, Barbara D

    The Journal of steroid biochemistry and molecular biology

    2023  Volume 232, Page(s) 106331

    Abstract: The role of vitamin D ...

    Abstract The role of vitamin D
    MeSH term(s) Humans ; Female ; Cholecalciferol/pharmacology ; 25-Hydroxyvitamin D3 1-alpha-Hydroxylase/genetics ; 25-Hydroxyvitamin D3 1-alpha-Hydroxylase/metabolism ; Vitamin D3 24-Hydroxylase/genetics ; Vitamin D3 24-Hydroxylase/metabolism ; Breast Neoplasms/drug therapy ; Estrogen Receptor alpha ; Vitamin D/pharmacology ; Vitamin D/metabolism ; Receptors, Calcitriol/metabolism
    Chemical Substances Cholecalciferol (1C6V77QF41) ; 25-Hydroxyvitamin D3 1-alpha-Hydroxylase (EC 1.14.15.18) ; Vitamin D3 24-Hydroxylase (EC 1.14.15.16) ; Estrogen Receptor alpha ; Vitamin D (1406-16-2) ; Receptors, Calcitriol ; CYP27B1 protein, human (EC 1.14.15.18) ; CYP24A1 protein, human (EC 1.14.15.16)
    Language English
    Publishing date 2023-05-25
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1049188-0
    ISSN 1879-1220 ; 0960-0760
    ISSN (online) 1879-1220
    ISSN 0960-0760
    DOI 10.1016/j.jsbmb.2023.106331
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  7. Article ; Online: New roles for dopamine D

    Farino, Zachary J / Morgenstern, Travis J / Maffei, Antonella / Quick, Matthias / De Solis, Alain J / Wiriyasermkul, Pattama / Freyberg, Robin J / Aslanoglou, Despoina / Sorisio, Denise / Inbar, Benjamin P / Free, R Benjamin / Donthamsetti, Prashant / Mosharov, Eugene V / Kellendonk, Christoph / Schwartz, Gary J / Sibley, David R / Schmauss, Claudia / Zeltser, Lori M / Moore, Holly /
    Harris, Paul E / Javitch, Jonathan A / Freyberg, Zachary

    Molecular psychiatry

    2019  Volume 25, Issue 9, Page(s) 2070–2085

    Abstract: ... mediated by DA D ...

    Abstract Although long-studied in the central nervous system, there is increasing evidence that dopamine (DA) has important roles in the periphery including in metabolic regulation. Insulin-secreting pancreatic β-cells express the machinery for DA synthesis and catabolism, as well as all five DA receptors. In these cells, DA functions as a negative regulator of glucose-stimulated insulin secretion (GSIS), which is mediated by DA D
    MeSH term(s) Animals ; Dopamine/metabolism ; Insulin Secretion ; Insulin-Secreting Cells/metabolism ; Mice ; Receptors, Dopamine D2/genetics ; Receptors, Dopamine D2/metabolism ; Receptors, Dopamine D3/genetics ; Receptors, Dopamine D3/metabolism
    Chemical Substances Receptors, Dopamine D2 ; Receptors, Dopamine D3 ; Dopamine (VTD58H1Z2X)
    Language English
    Publishing date 2019-01-09
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, N.I.H., Intramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 1330655-8
    ISSN 1476-5578 ; 1359-4184
    ISSN (online) 1476-5578
    ISSN 1359-4184
    DOI 10.1038/s41380-018-0344-6
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  8. Article ; Online: Effect of high dose vitamin D supplementation on subsequent immune responses to administration of the live herpes zoster vaccine to long-term care residents.

    Levin, Myron J / Ginde, Adit A / Schmid, D Scott / Lang, Nancy / Canniff, Jennifer / Schwartz, Robert S / Weinberg, Adriana

    Vaccine

    2024  Volume 42, Issue 9, Page(s) 2278–2281

    Abstract: ... in which they were randomized to receive either oral daily standard dose (400-1000 IU/day) 25-hydroxy vitamin D ...

    Abstract Thirty-three long-term care residents (mean age 76.5 years), who were participating in a study in which they were randomized to receive either oral daily standard dose (400-1000 IU/day) 25-hydroxy vitamin D (vitamin D3) (SD) or high dose (3000-4000 IU/day) (HD) vitamin D3, were vaccinated with the live, attenuated herpes zoster vaccine. Blood was drawn at vaccination and three weeks later to determine varicella-zoster virus (VZV) antibody and T-cell mediated immune responses. ELISA and neutralizing antibodies increased significantly, but to the same extent, in both groups. The antibody avidity significantly increased from pre- to post-vaccination only in the HD group. VZV-CMI, as measured by FLUOROSPOT significantly increased post-vaccination in both groups, but the difference in interferon-γ spot-forming cells (SFC) and interleukin-2 SFC was lower in the HD than SD group. The increase in VZV-CMI correlated inversely with circulating regulatory T cells in the HD group. We conclude that pre-treatment with HD vitamin D3 does not appreciably enhance the antibody response to a live vaccine and that VZV-CMI responses were diminished in HD vitamin D3 recipients.
    MeSH term(s) Humans ; Aged ; Herpes Zoster Vaccine ; Long-Term Care ; Immunity, Cellular ; Herpesvirus 3, Human ; Herpes Zoster/prevention & control ; Antibodies, Viral ; Vitamin D ; Cholecalciferol ; Vaccines, Attenuated ; Dietary Supplements
    Chemical Substances Herpes Zoster Vaccine ; Antibodies, Viral ; Vitamin D (1406-16-2) ; Cholecalciferol (1C6V77QF41) ; Vaccines, Attenuated
    Language English
    Publishing date 2024-02-28
    Publishing country Netherlands
    Document type Randomized Controlled Trial ; Journal Article
    ZDB-ID 605674-x
    ISSN 1873-2518 ; 0264-410X
    ISSN (online) 1873-2518
    ISSN 0264-410X
    DOI 10.1016/j.vaccine.2024.02.055
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  9. Article: [Full and D-Box-Deficient PTTG1 Isoforms: Effects on Cell Proliferation].

    Demin, D E / Stasevich, E M / Murashko, M M / Tkachenko, E A / Uvarova, A N / Schwartz, A M

    Molekuliarnaia biologiia

    2022  Volume 56, Issue 6, Page(s) 1104

    Abstract: ... exons encode the main recognition site (D-box) of the anaphase-promoting complex (APC/C). We show ... with a PTTG1-like set of APC/C recognition sites have known isoforms without the D-box. Overall, the data ...

    Abstract Human securin (PTTG1) is a protooncogene whose expression is elevated in many types of malignant cells. We previously discovered a minor short isoform of securin lacking exons 3 and 4. The missing exons encode the main recognition site (D-box) of the anaphase-promoting complex (APC/C). We show that these two PTTG1 isoforms have different effects on transcription. Here, we have studied the effects of overexpression and selective knockdown of the short and complete securin isoforms on cell proliferation using the xCELLigence system. Notably, selective knockdown of the short isoform mRNA led to a dramatic decrease in cell growth, while overexpression of both isoforms accelerated cell growth. To search for genes with alternative isoforms similar to securin, we analyzed the GENCODE database and found that 54 of 128 genes with a PTTG1-like set of APC/C recognition sites have known isoforms without the D-box. Overall, the data obtained indicate the existence of a new class of alternative isoforms and reinstates the importance of minor isoforms.
    MeSH term(s) Humans ; Protein Isoforms/genetics ; Cell Proliferation/genetics
    Chemical Substances Protein Isoforms
    Language Russian
    Publishing date 2022-12-07
    Publishing country Russia (Federation)
    Document type English Abstract ; Journal Article
    ZDB-ID 213542-5
    ISSN 0026-8984
    ISSN 0026-8984
    DOI 10.31857/S0026898422060076
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  10. Article ; Online: Structural rearrangements allow nucleic acid discrimination by type I-D Cascade.

    Schwartz, Evan A / McBride, Tess M / Bravo, Jack P K / Wrapp, Daniel / Fineran, Peter C / Fagerlund, Robert D / Taylor, David W

    Nature communications

    2022  Volume 13, Issue 1, Page(s) 2829

    Abstract: ... I-D interference proteins contain characteristic features of both type I and type III systems. Here ... we present the structures of type I-D Cascade bound to both a double-stranded (ds)DNA and a single-stranded ... ss)RNA target at 2.9 and 3.1 Å, respectively. We show that type I-D Cascade is capable ...

    Abstract CRISPR-Cas systems are adaptive immune systems that protect prokaryotes from foreign nucleic acids, such as bacteriophages. Two of the most prevalent CRISPR-Cas systems include type I and type III. Interestingly, the type I-D interference proteins contain characteristic features of both type I and type III systems. Here, we present the structures of type I-D Cascade bound to both a double-stranded (ds)DNA and a single-stranded (ss)RNA target at 2.9 and 3.1 Å, respectively. We show that type I-D Cascade is capable of specifically binding ssRNA and reveal how PAM recognition of dsDNA targets initiates long-range structural rearrangements that likely primes Cas10d for Cas3' binding and subsequent non-target strand DNA cleavage. These structures allow us to model how binding of the anti-CRISPR protein AcrID1 likely blocks target dsDNA binding via competitive inhibition of the DNA substrate engagement with the Cas10d active site. This work elucidates the unique mechanisms used by type I-D Cascade for discrimination of single-stranded and double stranded targets. Thus, our data supports a model for the hybrid nature of this complex with features of type III and type I systems.
    MeSH term(s) CRISPR-Associated Proteins/metabolism ; CRISPR-Cas Systems ; DNA/metabolism ; DNA Cleavage ; Nucleic Acids ; RNA
    Chemical Substances CRISPR-Associated Proteins ; Nucleic Acids ; RNA (63231-63-0) ; DNA (9007-49-2)
    Language English
    Publishing date 2022-05-20
    Publishing country England
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-022-30402-8
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