Evidence map›Paper›PMID 26595451›Full record

ArticleJournal of cellular physiology2016

The LPV Motif Is Essential for the Efficient Export of Secretory DMP1 From the Endoplasmic Reticulum.

Tian Liang, Tian Meng, Suzhen Wang, Chunlin Qin, Yongbo Lu

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Article
  3. 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

5 authors at 1 institution in 1 country.

Tian LiangDepartment of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas.
Tian MengDepartment of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas.
Suzhen WangDepartment of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas.
Chunlin QinDepartment of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas.
Yongbo LuDepartment of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas.
Texas A&M University · US

Funding

Studies of the Roles of DMP1 and DSPP in Osteogenesis and DentinogenesisR01DE005092 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI QIN, CHUNLIN · 1985 to 2012
$4.4M
Identification and Function of nuDMP1 in Odontoblast DifferentiationR01DE023365 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI LU, YONGBO · 2013 to 2016
$1.3M
STUDIES OF PROTEINS INVOLVED IN DENTINOGENESISR37DE005092 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BUTLER, WILLIAM T · 1987 to 1996
–
NIDCR NIH HHS DE005092NIDCR NIH HHS DE023365NIDCR NIH HHS R01 DE005092NIDCR NIH HHS R01 DE023365
6 · The paper itself

Abstract

Dentin matrix protein 1 (DMP1) is found abundantly in the extracellular matrices of bone and dentin. Secretory DMP1 begins with a tripeptide of leucine-proline-valine (LPV) after the endoplasmic reticulum (ER)-entry signal peptide is cleaved. The goal of this study was to determine the role of the LPV motif in the secretion of DMP1. A series of DNA constructs was generated to express various forms of DMP1 with or without the LPV motif. These constructs were transfected into a preosteoblast cell line, the MC3T3-E1 cells, and the subcellular localization and secretion of various forms of DMP1 were examined by immunofluorescent staining and Western-blotting analyses. Immunofluorescent staining showed that the LPV-containing DMP1 variants were primarily localized in the Golgi complex, whereas the LPV-lacking DMP1 variants were found abundantly within the ER. Western-blotting analyses demonstrated that the LPV-containing DMP1 variants were rapidly secreted from the transfected cells, as they did not accumulate within the cells, and the amounts increased in the conditioned media over time. In contrast, the LPV-lacking DMP1 variants were predominantly retained within the cells, and only small amounts were secreted out of the cells over time. These results suggest that the LPV motif is essential for the efficient export of secretory DMP1 from the ER to the Golgi complex.

Indexed as

3T3 CellsAmino Acid MotifsAnimalsDentinEndoplasmic ReticulumExtracellular Matrix ProteinsGolgi ApparatusHumansLeucineMiceOsteoblastsProlineValineDmp1 protein, mouseExtracellular Matrix ProteinsLeucineProlineValine

Identifiers

PMID26595451
PMCPMC4801704
OpenAlexW2179803147

What OpenQuestion holds

Textmetadata
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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.