Evidence map›Paper›PMID 24352500›Full record

ArticleJournal of dental research2014

DSPP contains an IRES element responsible for the translation of dentin phosphophoryn.

Y Zhang, Y Song, S Ravindran, Q Gao, C C Huang, A Ramachandran, A Kulkarni, A George

Abstract read
In one paragraph

Article in Journal of dental research, 2014. 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
1.8field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. The ER CaConnective tissue research · 2018
    Article
  10. Exosomes in Extracellular Matrix Bone Biology.Current osteoporosis reports · 2018
    Review
  11. Cancer Secretome May Influence BSP and DSP Expression in Human Salivary Gland Cells.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2017
    Article
  12. Article
  13. Article
  14. Dentin Matrix Proteins in Bone Tissue Engineering.Advances in experimental medicine and biology · 2015
    Review
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

8 authors at 2 institutions in 1 country.

Y ZhangBrodie Tooth Development Genetics & Regenerative Medicine Research Laboratory, Department of Oral Biology, University of Illinois at Chicago, Chicago, IL 60612, USA.
Y Song
S Ravindran
Q Gao
C C Huang
A Ramachandran
A Kulkarni
A George
University of Illinois Chicago · USNational Institute of Dental and Craniofacial Research · US

Funding

Intracellular and Extracellular function of dentin phosphophorynR01DE019633 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GEORGE, ANNE · 2010 to 2013
$1.5M
NIDCR NIH HHS R01 DE019633NIDCR NIH HHS R01 DE 19633
6 · The paper itself

Abstract

The major phosphoprotein in dentin is the aspartic acid and serine-rich protein called dentin phosphophoryn (DPP). DPP appears to be synthesized as a part of a larger compound protein, dentin sialophosphoprotein (DSPP). DSPP has never been isolated or detected in dentin extracts. It is now evident that DSPP is a chimeric protein composed of 3 parts: dentin sialoprotein (DSP), DPP, and dentin glycoprotein (DGP). Previous reports have suggested that the BMP1 protease is responsible for processing DSPP. However, unequal amounts of these products are present in the dentin matrix. Here, we provide evidence for an internal ribosome entry site in the DSPP gene that directs the synthesis of DPP. This mechanism would account for unequal amounts of intracellular DSP and DPP. The internal ribosomal entry site (IRES) activity varied in different cell types, suggesting the presence of additional regulatory elements during the translational regulation of DPP. Further, we provide evidence that DPP is transported to the extracellular matrix (ECM) through exosomes. Using tissue recombination and lentivirus-mediated gain-of-function approaches, we also demonstrate that DPP is essential for the formation of well-defined tooth structures with mineralized dentin matrix.

Indexed as

3T3 CellsAnimalsCell LineDental PulpDentinDentinogenesisDentin SialophosphoproteinExosomesExtracellular MatrixExtracellular Matrix ProteinsGenetic VectorsHEK293 CellsHumansLentivirusMaleMiceDentin SialophosphoproteinExtracellular Matrix ProteinsPhosphoproteinsSialoglycoproteinscell biologycell differentiationdentinextracellular matrix (ECM)matrix biologyodontoblast(s)

Identifiers

PMID24352500
PMCPMC3895336
OpenAlexW2093935724

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.