Evidence map›Paper›PMID 16492709›Full record

ArticleJournal of cell science2006

Sorting of Pmel17 to melanosomes through the plasma membrane by AP1 and AP2: evidence for the polarized nature of melanocytes.

Julio C Valencia, Hidenori Watabe, An Chi, Francois Rouzaud, Kevin G Chen, Wilfred D Vieira, Kaoruko Takahashi, Yuji Yamaguchi, Werner Berens, Kunio Nagashima and 4 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cell science, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Direct observation of the effects of chemical fixation in MNT-1 cells: A SE-ADM and Raman study.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  4. Melanosome Biogenesis in the Pigmentation of Mammalian Skin.Integrative and comparative biology · 2021
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Proprotein convertases process Pmel17 during secretion.The Journal of biological chemistry · 2011
    Article
  16. Glycoprotein nonmetastatic melanoma protein b, a melanocytic cell marker, is a melanosome-specific and proteolytically released protein.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
    Article
  17. The secreted form of a melanocyte membrane-bound glycoprotein (Pmel17/gp100) is released by ectodomain shedding.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
    Article
  18. Review
  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

14 authors at 3 institutions in 1 country.

Julio C ValenciaLaboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Hidenori Watabe
An Chi
Francois Rouzaud
Kevin G Chen
Wilfred D Vieira
Kaoruko Takahashi
Yuji Yamaguchi
Werner Berens
Kunio Nagashima
Jeffrey Shabanowitz
Donald F Hunt
Ettore Appella
Vincent J Hearing
National Institutes of Health · USNational Cancer Institute · USUniversity of Virginia · US

Funding

PROTEIN SEQUENCING BY TANDEM MASS SPECTROMETRYR01GM037537 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI HUNT, DONALD F · 1987 to 2023
$17.8M
MELANOMA AND MELANOGENESISZ01BC009100 · BC · BASIC SCIENCES · PI HEARING, VINCENT J · 1996 to 2006
–
Intramural NIH HHS Z99 NS999999NIGMS NIH HHS GM 37537NIGMS NIH HHS R01 GM037537
6 · The paper itself

Abstract

Adaptor proteins (AP) play important roles in the sorting of proteins from the trans-Golgi network, but how they function in the sorting of various melanosome-specific proteins such as Pmel17, an essential structural component of melanosomes, in melanocytes is unknown. We characterized the processing and trafficking of Pmel17 via adaptor protein complexes within melanocytic cells. Proteomics analysis detected Pmel17, AP1 and AP2, but not AP3 or AP4 in early melanosomes. Real-time PCR, immunolabeling and tissue in-situ hybridization confirmed the coexpression of AP1 isoforms mu1A and mu1B (expressed only in polarized cells) in melanocytes and keratinocytes, but expression of mu1B is missing in some melanoma cell lines. Transfection with AP1 isoforms (mu1A or mu1B) showed two distinct distribution patterns that involved Pmel17, and only mu1B was able to restore the sorting of Pmel17 to the plasma membrane in cells lacking mu1B expression. Finally, we established that expression of mu1B is regulated physiologically in melanocytes by UV radiation or DKK1. These results show that Pmel17 is sorted to melanosomes by various intracellular routes, directly or indirectly through the plasma membrane, and the presence of basolateral elements in melanocytes suggests their polarized nature.

Indexed as

Adaptor Protein Complex 1Adaptor Protein Complex 2Cell Line, TumorCell MembraneCell Polaritygp100 Melanoma AntigenHumansMelanocytesMelanosomesMembrane GlycoproteinsMicroscopy, ElectronProtein SubunitsProtein TransportSkinAdaptor Protein Complex 1Adaptor Protein Complex 2gp100 Melanoma AntigenMembrane GlycoproteinsPMEL protein, humanProtein Subunits

Identifiers

PMID16492709
PMCPMC4629779
OpenAlexW2147898185

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.