Evidence map›Paper›PMID 11074006›Full record

ArticleMolecular and cellular biology2000

Heterogeneous nuclear ribonucleoproteins C1 and C2 associate with the RNA component of human telomerase.

L P Ford, J M Suh, W E Wright, J W Shay

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.3field-weighted citation impact, top 5% of its field
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

33 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
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  10. Expression profile of telomere-associated genes in multiple myeloma.Journal of cellular and molecular medicine · 2012
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. The biogenesis and regulation of telomerase holoenzymes.Nature reviews. Molecular cell biology · 2006
    Review
  18. In vivo identification of ribonucleoprotein-RNA interactions.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

L P FordDepartment of Cell Biology, The University of Texas Southwestern Medical Center, Dallas, Texas 75390-9039, USA.
J M Suh
W E Wright
J W Shay
The University of Texas Southwestern Medical Center · US

Funding

GENE EXPRESSION IN AGING AND DEVELOPMENTR01AG001228 · NIA · UT SOUTHWESTERN MEDICAL CENTER · PI SHAY, JERRY WILLIAM · 1985 to 2018
$7.6M
MECHANISMS OF CELLULAR IMMORTALIZATIONR01AG007992 · NIA · UT SOUTHWESTERN MEDICAL CENTER · PI WRIGHT, WOODRING ERIK · 1989 to 2010
$3.3M
GENE EXPRESSION IN AGING AND DEVELOPMENTR37AG001228 · NIA · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI WRIGHT, WOODRING ERIK · 1987 to 1996
–
MULTIDISCIPLINARY ONCOLOGY TRAINING GRANTT32CA066187 · NCI · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI HUTH, JAMES F. · 1995 to 1999
–
NCI NIH HHS T32 CA066187NCI NIH HHS T32-CA66187NIA NIH HHS AG01228NIA NIH HHS AG07992NIA NIH HHS R01 AG001228NIA NIH HHS R01 AG007992
6 · The paper itself

Abstract

Here we demonstrate that heterogeneous nuclear ribonucleoproteins (hnRNPs) C1 and C2 can associate directly with the integral RNA component of mammalian telomerase. The binding site for hnRNPs C1 and C2 maps to a 6-base uridylate tract located directly 5' to the template region in the human telomerase RNA (TR) and a 4-base uridylate tract directly 3' to the template in the mouse TR. Telomerase activity is precipitated with antibodies specific to hnRNPs C1 and C2 from cells expressing wild-type human TR but not a variant of the human TR lacking the hnRNPs C1 and C2 binding site, indicating that hnRNPs C1 and C2 require the 6-base uridylate tract within the human TR to associate with the telomerase holoenzyme. In addition, we demonstrate that binding of hnRNPs C1 and C2 to telomerase correlates with the ability of telomerase to access the telomere. Although correlative, these data do suggest that the binding of hnRNPs C1 and C2 to telomerase may be important for the ability of telomerase to function on telomeres. The C proteins of the hnRNP particle are also capable of colocalizing with telomere binding proteins, suggesting that the C proteins may associate with telomeres in vivo. Therefore, human telomerase is capable of associating with core members of the hnRNP family of RNA binding proteins through a direct and sequence-specific interaction with the human TR. This is also the first account describing the precise mapping of a sequence in the human TR that is required to associate with an auxiliary component of the human telomerase holoenzyme.

Indexed as

Heterogeneous-Nuclear Ribonucleoprotein Group CBase SequenceBinding SitesHeterogeneous-Nuclear RibonucleoproteinsHumansMolecular Sequence DataMutagenesis, Site-DirectedProtein BindingRibonucleoproteinsRNARNA, Long NoncodingRNA, UntranslatedTelomeraseTelomereC1 HNRNPHeterogeneous-Nuclear Ribonucleoprotein Group CHeterogeneous-Nuclear RibonucleoproteinsHNRNPC protein, humanHnrnpc protein, mouseRibonucleoproteinsRNARNA, Long NoncodingRNA, UntranslatedTelomerasetelomerase RNA

Identifiers

PMID11074006
PMCPMC86561
OpenAlexW2121743146

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.