Evidence map›Paper›PMID 25451932›Full record

ArticleThe Journal of biological chemistry2015

Distinct roles of N-glycosylation at different sites of corin in cell membrane targeting and ectodomain shedding.

Hao Wang, Tiantian Zhou, Jianhao Peng, Ping Xu, Ningzheng Dong, Shenghan Chen, Qingyu Wu

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. N-Glycan-calnexin interactions in human factor VII secretion and deficiency.The international journal of biochemistry & cell biology · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Role of corin in the regulation of blood pressure.Current opinion in nephrology and hypertension · 2017
    Review
  17. Article
  18. Review
  19. A novel cytoplasmic tail motif regulates mouse corin expression on the cell surface.Biochemical and biophysical research communications · 2015
    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

7 authors at 3 institutions in 2 countries.

Hao WangFrom the Department of Molecular Cardiology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, the Department of Chemistry, Cleveland State University, Cleveland, Ohio 44115, and.
Tiantian Zhouthe Cyrus Tang Hematology Center and Collaborative Innovation Center of Hematology, Soochow University, Suzhou 215123, China.
Jianhao PengFrom the Department of Molecular Cardiology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.
Ping XuFrom the Department of Molecular Cardiology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.
Ningzheng Dongthe Cyrus Tang Hematology Center and Collaborative Innovation Center of Hematology, Soochow University, Suzhou 215123, China.
Shenghan ChenFrom the Department of Molecular Cardiology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195.
Qingyu WuFrom the Department of Molecular Cardiology, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, the Department of Chemistry, Cleveland State University, Cleveland, Ohio 44115, and the Cyrus Tang Hematology Center and Collaborative Innovation Center of Hematology, Soochow University, Suzhou 215123, China wuq@ccf.org.
Cleveland Clinic Lerner College of Medicine · USSoochow University · CNCleveland State University · US

Funding

The cardiac protease corin in natriuretic peptide processing and hypertensionR01HL089298 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI WU, QINGYU · 2008 to 2012
$2.2M
Serine Protease Corin in Pregnancy-induced HypertensionR01HD064634 · NICHD · CLEVELAND CLINIC LERNER COM-CWRU · PI WU, QINGYU · 2011 to 2015
$1.6M
NHLBI NIH HHS HL089298NHLBI NIH HHS R01 HL089298NICHD NIH HHS HD064634NICHD NIH HHS R01 HD064634
6 · The paper itself

Abstract

Corin is a membrane-bound protease essential for activating natriuretic peptides and regulating blood pressure. Human corin has 19 predicted N-glycosylation sites in its extracellular domains. It has been shown that N-glycans are required for corin cell surface expression and zymogen activation. It remains unknown, however, how N-glycans at different sites may regulate corin biosynthesis and processing. In this study, we examined corin mutants, in which each of the 19 predicted N-glycosylation sites was mutated individually. By Western analysis of corin proteins in cell lysate and conditioned medium from transfected HEK293 cells and HL-1 cardiomyocytes, we found that N-glycosylation at Asn-80 inhibited corin shedding in the juxtamembrane domain. Similarly, N-glycosylation at Asn-231 protected corin from autocleavage in the frizzled-1 domain. Moreover, N-glycosylation at Asn-697 in the scavenger receptor domain and at Asn-1022 in the protease domain is important for corin cell surface targeting and zymogen activation. We also found that the location of the N-glycosylation site in the protease domain was not critical. N-Glycosylation at Asn-1022 may be switched to different sites to promote corin zymogen activation. Together, our results show that N-glycans at different sites may play distinct roles in regulating the cell membrane targeting, zymogen activation, and ectodomain shedding of corin.

Indexed as

GlycosylationMutationAnimalsAtrial Natriuretic FactorCell MembraneEnzyme PrecursorsFlow CytometryGlycoside HydrolasesHEK293 CellsHumansMiceModels, MolecularMyocytes, CardiacPlasmidsProtein BindingProtein Structure, TertiaryAtrial Natriuretic FactorCORIN protein, humanCorin protein, mouseEnzyme PrecursorsGlycoside HydrolasesSerine EndopeptidasesCorinEctodomain SheddingIntracellular TraffickingMembrane ProteaseN-Linked GlycosylationProteolytic EnzymeSerine ProteaseShedding

Identifiers

PMID25451932
PMCPMC4340409
OpenAlexW2005100755

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.