Evidence map›Paper›PMID 26324849›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2016

Family with sequence similarity member 20C is the primary but not the only kinase for the small-integrin-binding ligand N-linked glycoproteins in bone.

Xiudong Yang, Wenjuan Yan, Ye Tian, Pan Ma, Lynne A Opperman, Xiaofang Wang

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

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  2. The phosphorylation of serineMatrix biology : journal of the International Society for Matrix Biology · 2022
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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

6 authors at 4 institutions in 2 countries.

Xiudong Yang*Department of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas, USA; Southern Medical University, Guangdong, People's Republic of China; Sichuan University, Sichuan, People's Republic of China; and Capital Medical University, Beijing, People's Republic of China.
Wenjuan Yan*Department of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas, USA; Southern Medical University, Guangdong, People's Republic of China; Sichuan University, Sichuan, People's Republic of China; and Capital Medical University, Beijing, People's Republic of China.
Ye Tian*Department of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas, USA; Southern Medical University, Guangdong, People's Republic of China; Sichuan University, Sichuan, People's Republic of China; and Capital Medical University, Beijing, People's Republic of China.
Pan Ma*Department of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas, USA; Southern Medical University, Guangdong, People's Republic of China; Sichuan University, Sichuan, People's Republic of China; and Capital Medical University, Beijing, People's Republic of China.
Lynne A Opperman*Department of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas, USA; Southern Medical University, Guangdong, People's Republic of China; Sichuan University, Sichuan, People's Republic of China; and Capital Medical University, Beijing, People's Republic of China.
Xiaofang Wang*Department of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas, USA; Southern Medical University, Guangdong, People's Republic of China; Sichuan University, Sichuan, People's Republic of China; and Capital Medical University, Beijing, People's Republic of China xwang@bcd.tamhsc.edu.
International Craniofacial Institute · USBaylor University · USTexas A&M University · USTexas A&M University System · US

Funding

Role of FAM20C in the Phosphorylation of SIBLING ProteinR03DE023873 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI WANG, XIAOFANG · 2014 to 2015
$218k
NIDCR NIH HHS R03 DE023873NIDCR NIH HHS R03DE23873-01
6 · The paper itself

Abstract

Recent studies have identified family with sequence similarity member 20C (FAM20C) as a kinase that phosphorylates the Ser in Ser-X-Glu/phospho-Ser (pSer) motifs in the small-integrin-binding ligand N-linked glycoproteins (SIBLINGs). There is no in vivo evidence that validates this finding, and it is unclear whether FAM20C is the only kinase for SIBLINGs. We extracted bone noncollagenous proteins (NCPs) from Fam20C-knockout (KO) mice and analyzed the phosphorylation levels. The total NCPs were separated into osteopontin-, bone sialoprotein-, and dentin matrix protein-1-enriched fractions by anion-exchange chromatography and analyzed by SDS-PAGE, native PAGE, and Western immunoblot analysis. The NCP phosphorylation level in the KO mice was lower than that in the wild-type (WT). On the native gel, the SIBLINGs from KO mice showed a lower migration rate (Mr) than those from the WT. Calf intestine phosphatase treatment shifted SIBLINGs from the WT mice to the level adjacent to the KO, but failed to shift the latter, suggesting a phosphorylation loss of SIBLINGs in the KO mice. Mass spectrometry identified less pSers in the SIBLINGs from the KO mice [including the region of the acidic Ser- and aspartate-rich motif (ASARM) peptides]. In an intriguing finding, several pSers in the Ser-X-Glu motifs in the KO mice maintained their phosphorylation, whereas several others in non-Ser-X-Glu motifs did not. Phospho-Tyrs and phospho-Thrs in the SIBLINGs did not appear to be associated with FAM20C. Our results indicate that FAM20C is the primary, but not the only, kinase for the SIBLINGs.-Yang, X., Yan, W., Tian, Y., Ma, P., Opperman, L. A., Wang, X. Family with sequence similarity member 20C is the primary but not the only kinase for the small-integrin-binding ligand N-linked glycoproteins in bone.

Indexed as

AnimalsBone and BonesCalcification, PhysiologicCalcium-Binding ProteinsCattleElectrophoresis, Polyacrylamide GelExtracellular Matrix ProteinsIntegrinsMice, KnockoutOsteopontinPHEX Phosphate Regulating Neutral EndopeptidaseCalcium-Binding ProteinsExtracellular Matrix ProteinsFAM20C protein, mouseIntegrinsOsteopontinPHEX Phosphate Regulating Neutral EndopeptidaseASARMbiomineralizationhypophosphatemic ricketsmass spectrometryphosphorylation

Identifiers

PMID26324849
PMCPMC4684535
OpenAlexW2228085709

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.