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  1. Article ; Online: FMRP regulates mRNAs encoding distinct functions in the cell body and dendrites of CA1 pyramidal neurons.

    Hale, Caryn R / Sawicka, Kirsty / Mora, Kevin / Fak, John J / Kang, Jin Joo / Cutrim, Paula / Cialowicz, Katarzyna / Carroll, Thomas S / Darnell, Robert B

    eLife

    2021  Volume 10

    Abstract: Neurons rely on translation of synaptic mRNAs in order to generate activity-dependent changes in plasticity. Here, we develop a strategy combining compartment-specific crosslinking immunoprecipitation (CLIP) and translating ribosome affinity purification ...

    Abstract Neurons rely on translation of synaptic mRNAs in order to generate activity-dependent changes in plasticity. Here, we develop a strategy combining compartment-specific crosslinking immunoprecipitation (CLIP) and translating ribosome affinity purification (TRAP) in conditionally tagged mice to precisely define the ribosome-bound dendritic transcriptome of CA1 pyramidal neurons. We identify CA1 dendritic transcripts with differentially localized mRNA isoforms generated by alternative polyadenylation and alternative splicing, including many that have altered protein-coding capacity. Among dendritic mRNAs, FMRP targets were found to be overrepresented. Cell-type-specific FMRP-CLIP and TRAP in microdissected CA1 neuropil revealed 383 dendritic FMRP targets and suggests that FMRP differentially regulates functionally distinct modules in CA1 dendrites and cell bodies. FMRP regulates ~15-20% of mRNAs encoding synaptic functions and 10% of chromatin modulators, in the dendrite and cell body, respectively. In the absence of FMRP, dendritic FMRP targets had increased ribosome association, consistent with a function for FMRP in synaptic translational repression. Conversely, downregulation of FMRP targets involved in chromatin regulation in cell bodies suggests a role for FMRP in stabilizing mRNAs containing stalled ribosomes in this compartment. Together, the data support a model in which FMRP regulates the translation and expression of synaptic and nuclear proteins within different compartments of a single neuronal cell type.
    MeSH term(s) Animals ; Cell Body/physiology ; Dendrites/physiology ; Female ; Fragile X Mental Retardation Protein/genetics ; Gene Expression Regulation ; Male ; Mice ; Mice, Inbred C57BL ; Neuronal Plasticity/physiology ; Pyramidal Cells/classification ; Pyramidal Cells/physiology ; RNA, Messenger/genetics ; Transcriptome
    Chemical Substances RNA, Messenger ; Fragile X Mental Retardation Protein (139135-51-6)
    Language English
    Publishing date 2021-12-23
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2687154-3
    ISSN 2050-084X ; 2050-084X
    ISSN (online) 2050-084X
    ISSN 2050-084X
    DOI 10.7554/eLife.71892
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: DRUL for school: Opening Pre-K with safe, simple, sensitive saliva testing for SARS-CoV-2.

    Frank, Mayu O / Blachere, Nathalie E / Parveen, Salina / Hacisuleyman, Ezgi / Fak, John / Luna, Joseph M / Michailidis, Eleftherios / Wright, Samara / Stark, Pamela / Campbell, Ann / Foo, Ashley / Sakmar, Thomas P / Huffman, Virginia / Bergh, Marissa / Goldfarb, Audrey / Mansisidor, Andres / Patriotis, Agata L / Palmquist, Karl H / Poulton, Nicolas /
    Leicher, Rachel / Vargas, César D M / Duba, Irene / Hurley, Arlene / Colagreco, Joseph / Pagane, Nicole / Orange, Dana E / Mora, Kevin / Rakeman, Jennifer L / Fowler, Randal C / Fernandes, Helen / Lamendola-Essel, Michelle F / Didkovsky, Nicholas / Silvera, Leopolda / Masci, Joseph / Allen, Machelle / Rice, Charles M / Darnell, Robert B

    PloS one

    2021  Volume 16, Issue 6, Page(s) e0252949

    Abstract: To address the need for simple, safe, sensitive, and scalable SARS-CoV-2 tests, we validated and implemented a PCR test that uses a saliva collection kit use at home. Individuals self-collected 300 μl saliva in vials containing Darnell Rockefeller ... ...

    Abstract To address the need for simple, safe, sensitive, and scalable SARS-CoV-2 tests, we validated and implemented a PCR test that uses a saliva collection kit use at home. Individuals self-collected 300 μl saliva in vials containing Darnell Rockefeller University Laboratory (DRUL) buffer and extracted RNA was assayed by RT-PCR (the DRUL saliva assay). The limit of detection was confirmed to be 1 viral copy/μl in 20 of 20 replicate extractions. Viral RNA was stable in DRUL buffer at room temperature up to seven days after sample collection, and safety studies demonstrated that DRUL buffer immediately inactivated virus at concentrations up to 2.75x106 PFU/ml. Results from SARS-CoV-2 positive nasopharyngeal (NP) swab samples collected in viral transport media and assayed with a standard FDA Emergency Use Authorization (EUA) test were highly correlated with samples placed in DRUL buffer. Direct comparison of results from 162 individuals tested by FDA EUA oropharyngeal (OP) or NP swabs with co-collected saliva samples identified four otherwise unidentified positive cases in DRUL buffer. Over six months, we collected 3,724 samples from individuals ranging from 3 months to 92 years of age. This included collecting weekly samples over 10 weeks from teachers, children, and parents from a pre-school program, which allowed its safe reopening while at-risk pods were quarantined. In sum, we validated a simple, sensitive, stable, and safe PCR-based test using a self-collected saliva sample as a valuable tool for clinical diagnosis and screening at workplaces and schools.
    MeSH term(s) COVID-19/diagnosis ; COVID-19/genetics ; COVID-19 Nucleic Acid Testing ; Child ; Female ; Humans ; Male ; SARS-CoV-2 ; Saliva/virology ; Schools ; Specimen Handling
    Language English
    Publishing date 2021-06-25
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0252949
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: DRUL for School: Opening Pre-K with safe, simple, sensitive saliva testing for SARS-CoV-2

    Frank, Mayu / Blachere, Nathalie E / Parveen, Salina / Hacisuleyman, Ezgi / Fak, John / Luna, Joseph M / Michailidis, Eleftherios / Wright, Samara / Stark, Pamela / Campbell, Ann H / Foo, Ashley / Sakmar, Thomas P / Huffman, Virginia / Bergh, Marissa / Goldfarb, Audrey / Mansisidor, Andrew / Patriotis, Agata L / Palmquist, Karl H / Poulton, Nicolas /
    Leicher, Rachel / Vargas, Cesar D / Duba, Irene / Hurley, Arlene / Colagreco, Joseph P / Pagane, Nicole / Orange, Dana E / Mora, Kevin / Rakeman, Jennifer L / Fowler, Randal C / Fernandes, Helen / Lamendola-Essel, Michelle F / Didkovsky, Nick / Silvera, Leopolda / Masci, Joseph / Allen, Machelle / Rice, Charles M / Darnell, Robert B

    medRxiv

    Abstract: To address the need for simple, safe, sensitive, and scalable SARS-CoV-2 tests, we validated and implemented a PCR test that uses a saliva collection kit use at home. Individuals self-collected 300 ul saliva in vials containing Darnell Rockefeller ... ...

    Abstract To address the need for simple, safe, sensitive, and scalable SARS-CoV-2 tests, we validated and implemented a PCR test that uses a saliva collection kit use at home. Individuals self-collected 300 ul saliva in vials containing Darnell Rockefeller University Laboratory (DRUL) buffer and extracted RNA was assayed by RT-PCR (the DRUL saliva assay). The limit of detection was confirmed to be 1 viral copy/ul in 20 of 20 replicate extractions. Viral RNA was stable in DRUL buffer at room temperature up to seven days after sample collection, and safety studies demonstrated that DRUL buffer immediately inactivated virus at concentrations up to 2.75x106 PFU/ml. Results from SARS-CoV-2 positive nasopharyngeal (NP) swab samples collected in viral transport media and assayed with a standard FDA Emergency Use Authorization (EUA) test were highly correlated with samples placed in DRUL buffer. Direct comparison of results from 162 individuals tested by FDA EUA oropharyngeal (OP) or NP swabs with co-collected saliva samples identified four otherwise unidentified positive cases in DRUL buffer. Over six months, we collected 3,724 samples from individuals ranging from 3 months to 92 years of age. This included collecting weekly samples over 10 weeks from teachers, children, and parents from a pre-school program, which allowed its safe reopening while at-risk pods were quarantined. In sum, we validated a simple, sensitive, stable, and safe PCR-based test using a self-collected saliva sample as a valuable tool for clinical diagnosis and screening at workplaces and schools.
    Keywords covid19
    Language English
    Publishing date 2021-04-06
    Publisher Cold Spring Harbor Laboratory Press
    Document type Article ; Online
    DOI 10.1101/2021.04.03.21254873
    Database COVID19

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