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Cloning of cDNAs Encoding Two Related 100-kD Coated Vesicle Proteins (α-Adaptins)

Margaret S. Robinson
The Journal of Cell Biology
Vol. 108, No. 3 (Mar., 1989), pp. 833-842
Stable URL: http://www.jstor.org/stable/1613377
Page Count: 10
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Cloning of cDNAs Encoding Two Related 100-kD Coated Vesicle Proteins (α-Adaptins)
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Abstract

Coat proteins of ∼100-kD (adaptins) are components of the adaptor complexes which link clathrin to receptors in coated vesicles. The α-adaptins, which are found exclusively in endocytic coated vesicles, separate into two bands on SDS gels, designated A and C. Two distinct cDNAs (sequences 1 and 2) encoding the two α-adaptins were cloned from a mouse brain cDNA library. Southern blotting indicates that there is one copy of each of the two α-adaptin genes, and that there are no additional closely related genes. Based on the size of the predicted protein products of the two genes (108 and 104 kD), the relative abundance of the two messages in brain and liver, and the reactivity of a sequence 1 fusion protein with different antibodies, it was possible to conclude that sequence 1 codes for A and sequence 2 for C. The two protein sequences are strikingly homologous to each other (84% identical amino acids), the major difference being an additional stretch of 41 amino acids, rich in prolines and acidic residues, inserted into the COOH-terminal half of A. In situ hybridization carried out on mouse brain sections indicates that the same cell type may express both transcripts, but that their relative expressions vary. Antipeptide antibodies are now being raised to find out whether the proteins are localized in functionally distinct populations of endocytic coated vesicles.

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