Cited by 273Autophagy in Disease and TherapyUbiquitin and proteasome pathwaysCellular transport and secretion

Post-translational Modifications of Three Members of the Human MAP1LC3 Family and Detection of a Novel Type of Modification for MAP1LC3B

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He, Hua, Dang, Yongjun, Dai, Fangyan, Guo, Zekun, Wu, Jiaxue, She, Xinyu, Pei, Yuan, Chen, Yongjing +5 more·2003·Journal of Biological Chemistry

Abstract

The molecular machinery required for autophagy is highly conserved in all eukaryotes as seen by the high degree of conservation of proteins involved in the formation of the autophagosome membranes. Recently, both yeast Apg8p and its rat homologue Map1lc3 were identified as essential constituents of autophagosome membrane as a processed form. In addition, both the yeast and human proteins exist in two modified forms produced by a series of post-translational modifications including a critical C-terminal cleavage after a conserved Gly residue, and the smaller processed form is associated with the autophagosome membranes. Herein, we report the identification and characterization of three human orthologs of the rat Map1LC3, named MAP1LC3A, MAP1LC3B, and MAP1LC3C. We show that the three isoforms of human MAP1LC3 exhibit distinct expression patterns in different human tissues. Importantly, we found that the three isoforms of MAP1LC3 differ in their post-translation modifications. Although MAP1LC3A and MAP1LC3C are produced by the proteolytic cleavage after the conserved C-terminal Gly residue, like their rat counterpart, MAP1LC3B does not undergo C-terminal cleavage and exists in a single modified form. The essential site for the distinct post-translation modification of MAP1LC3B is Lys-122 rather than the conserved Gly-120. Subcellular localization by cell fractionation and immunofluorescence revealed that three human isoforms are associated with membranes involved in the autophag…

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Crossref · 10.1074/jbc.m303800200

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  • The first LC3 subfamily comprises LC3A (including 2 splicing variants), LC3B and LC3C.

    “The first LC3 subfamily comprises LC3A (including 2 splicing variants), LC3B and LC3C [28].”
  • The use of imaging cytometry allows rapid and quantitative measures of the number of LC3 puncta and their relative number in individual or mixed cell types, using computerized assessment, enumeration, and data display.

    “The use of imaging cytometry allows rapid and quantitative measures of the number of LC3 puncta and their relative number in individual or mixed cell types, using computerized assessment, enumeration, and data display (e.g., see refs.142 and 210).”

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Authors
He, H., Dang, Y., Dai, F., Guo, Z., Wu, J., She, X., Pei, Y., Chen, Y., Ling, W., Wu, C., Zhao, S., Liu, J. O., & Yu, L.
Affiliations
  • Fudan University (CN)
  • Johns Hopkins University (US)
Corresponding author
Yu, Long
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
2003-08
Volume
278
Issue
31
Pages
29278-29287
ISSN
0021-9258 (ISSN-L)
OpenAlex
W2111892050
Cited by
273
References
2
Citations by year
2026: 1 · 2025: 6 · 2024: 11 · 2023: 11 · 2022: 10 · 2021: 19 · 2020: 16 · 2019: 11 · 2018: 15 · 2017: 12 · 2016: 22 · 2015: 15 · 2014: 11 · 2013: 29 · 2012: 18
FWCI
3.99
Type
journal article
Language
en
Open access
Locations
  • Journal of Biological Chemistry (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
Keywords
LC3, MAP1LC3A, LC3B, autophagy, post-translational modification, C-terminal cleavage, lysine modification, subcellular localization
MeSH terms
Amino Acid Sequence, Animals, Base Sequence, Cell Line, Cloning, Molecular, Escherichia coli, Fluorescent Antibody Technique, Glycine, HeLa Cells, Humans, Kidney, Lysine, Microscopy, Fluorescence, Microtubule-Associated Proteins, Molecular Sequence Data, Peptide Fragments, Protein Processing, Post-Translational, Saccharomyces cerevisiae, Transfection, Blotting, Northern, Gene Expression, Mutagenesis, Site-Directed, Sequence Alignment, Gene Deletion, Protein Isoforms, Mice, Rats

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