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PMID: 8308025 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Differential expression and regulation of multiple dynamins.

The Journal of biological chemistry ·Vol. 269 ·No. 6 ·1994-02-11 ·Pages 4547-54

Sontag JM, Fykse EM, Ushkaryov Y, Liu JP, Robinson PJ, Südhof TC

Abstract

Dynamin is a GTP-, microtubule-, and phospholipid-binding protein that is expressed primarily in brain. In Drosophila, the shibire gene encodes a homologue of dynamin; mutations in this gene result in a defect in endocytosis, suggesting a function for dynamin in endocytic membrane traffic. In the present study we show that there are at least two distinct dynamin genes in mammals whose products are referred to as dynamins I and II. The two dynamins are similar to each other (79% identity) and are both equally homologous to the Drosophila shibire gene product (66% identity). The highest degree of identity between dynamins is observed in their N-terminal halves, whereas their C termini exhibit little homology. Transcripts of both dynamin genes are subject to at least two alternative splicing events, the first of which is identically found in both dynamins, whereas the second site of alternative splicing is different between the two types of dynamins. The first alternatively spliced sequence of the dynamins consists of an interior region that is present in two distinct but homologous forms in both dynamins, suggesting alternative use of exons in both genes at identical positions. The second site of alternative splicing results in the generation of different C termini in dynamin I and in the inclusion or exclusion of an interior four-amino acid sequence in dynamin II. The two dynamins exhibit remarkable differences in their tissue distribution and regulation. Dynamin I is almost exclusively expressed in the central nervous system. Conversely, dynamin II is expressed ubiquitously in all tissues tested. Previous studies revealed that the GTPase activity of dynamin I is regulated by phosphorylation by protein kinase C in nerve terminals. Expression of dynamins I and II by transfection in COS cells demonstrates that only dynamin I but not dynamin II is a substrate for protein kinase C. Our data suggest a specialization in the endocytic functions and the regulation of dynamins between neural and non-neural tissues in mammals.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Cloning, Molecular DNA Primers/chemistry Drosophila Proteins Dynamin I Dynamins GTP Phosphohydrolases/genetics,metabolism Genes Genes, Insect Molecular Sequence Data Phosphoproteins/genetics,metabolism Phosphorylation Protein Kinase C/metabolism Rats Sequence Alignment Sequence Homology, Amino Acid Sequence Homology, Nucleic Acid Tissue Distribution
Chemicals
DNA Primers Drosophila Proteins Phosphoproteins Protein Kinase C Dynamin I GTP Phosphohydrolases Dynamins shi protein, Drosophila
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Sontag J M
Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas 75235.
Fykse E M
Ushkaryov Y
Liu J P
Robinson P J
Südhof T C
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1994-02-11
Pages
4547-54
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
GENBANK
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