Evidence map›Paper›PMID 30357357›Full record

ArticleNucleic acids research2018

Single-cell stabilization method identifies gonadotrope transcriptional dynamics and pituitary cell type heterogeneity.

Frederique Ruf-Zamojski, Yongchao Ge, Venugopalan Nair, Michel Zamojski, Hanna Pincas, Chirine Toufaily, Jessica Tome-Garcia, Marlon Stoeckius, William Stephenson, Gregory R Smith and 8 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Imaging of Endoplasmic Reticulum CaFrontiers in endocrinology · 2020
    Article
  10. Article
  11. Using single-cell transcriptomics to understand functional states and interactions in microbial eukaryotes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Article
  12. Review
  13. Article
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Frederique Ruf-ZamojskiDepartment of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Yongchao GeDepartment of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Venugopalan NairDepartment of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Michel ZamojskiDepartment of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Hanna PincasDepartment of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Chirine ToufailyDept. of Pharmacology and Therapeutics, McGill University, Montreal, Quebec H3G 1Y6, Canada.
Jessica Tome-GarciaDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Marlon StoeckiusNew York Genome Center, New York, NY 10013, USA.
William StephensonNew York Genome Center, New York, NY 10013, USA.
Gregory R SmithDepartment of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Daniel J BernardDept. of Pharmacology and Therapeutics, McGill University, Montreal, Quebec H3G 1Y6, Canada.
Nadejda M TsankovaDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Boris M HartmannDepartment of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Miguel FribourgDepartment of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Peter SmibertNew York Genome Center, New York, NY 10013, USA.
Harold SwerdlowNew York Genome Center, New York, NY 10013, USA.
Judith L TurgeonDepartment of Internal Medicine, University of California, Davis, CA 95616, USA.
Stuart C SealfonDepartment of Neurology, Center for Advanced Research on Diagnostic Assays, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Funding

Structure based design of antibodies and vaccinesU19AI117905 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SCHIEF, WILLIAM R. · 2015 to 2019
$12.0M
MOLECULAR MECHANISM OF AGONISM AT THE GNRH RECEPTORR01DK046943 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI STUART C. SEALFON · 1993 to 2026
$11.0M
Project I: Immunity to Influenza in Primary Lung Epithelial CellsU19AI117873 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SEALFON, STUART C. · 2015 to 2019
$8.6M
Transforming Genomics with 5 PB Big Omics Data Engine Cray CS300-AC SupercomputerS10OD018522 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2014 to 2014
$1.9M
Integrated systems biology of the pituitaryR56DK046943 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SEALFON, STUART C. · 2006 to 2024
$555k
CIHR MOP-123447NIAID NIH HHS U19 AI117873NIAID NIH HHS U19 AI117905NIDDK NIH HHS R01 DK046943NIDDK NIH HHS R56 DK046943NIH HHS S10 OD018522
6 · The paper itself

Abstract

Immediate-early response genes (IEGs) are rapidly and transiently induced following an extracellular signal. Elucidating the IEG response patterns in single cells (SCs) requires assaying large numbers of timed samples at high accuracy while minimizing handling effects. To achieve this, we developed and validated RNA stabilization Buffer for Examination of Single-cell Transcriptomes (RNA-Best), a versatile single-step cell and tissue preservation protocol that stabilizes RNA in intact SCs without perturbing transcription patterns. We characterize for the first time SC heterogeneity in IEG responses to pulsatile gonadotropin-releasing hormone (GnRH) stimuli in pituitary gonadotrope cells. Our study identifies a gene-specific hierarchical pattern of all-or-none transcript induction elicited by increasing concentrations of GnRH. This quantal pattern of gene activation raises the possibility that IEG activation, when accurately resolved at the SC level, may be mediated by gene bits that behave as pure binary switches.

Indexed as

AnimalsBuffersCell Line, TumorDose-Response Relationship, DrugEarly Growth Response Protein 1Early Growth Response Protein 2Genes, Immediate-EarlyGenetic HeterogeneityGonadotrophsGonadotropin-Releasing HormoneMiceProto-Oncogene Proteins c-fosRNA, MessengerRNA StabilitySequence Analysis, RNASingle-Cell AnalysisBuffersEarly Growth Response Protein 1Early Growth Response Protein 2Egr1 protein, mouseEgr2 protein, mouseFosb protein, mouseGonadotropin-Releasing HormoneProto-Oncogene Proteins c-fosRNA, Messenger

Identifiers

PMID30357357
PMCPMC6265460

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.