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Sarco/endoplasmic-reticulum calcium ATPase SERCA1 is maintained in the endoplasmic reticulum by a retrieval signal located between residues 1 and 211.
- Source :
-
The Biochemical journal [Biochem J] 2003 May 01; Vol. 371 (Pt 3), pp. 775-82. - Publication Year :
- 2003
-
Abstract
- The location of sarco/endoplasmic-reticulum calcium ATPase (SERCA) retention/retrieval motifs in the sequence of the SERCA1 has been investigated by examining the subcellular location in COS-7 cells of enhanced-green-fluorescent-protein-tagged calcium-pump chimaeras. These chimaeras have been constructed from the fast-twitch SERCA1 and the plasma-membrane calcium ATPase PMCA3. The N-terminal, central and C-terminal segments of these calcium pumps were exchanged between SERCA1 and PMCA3. The segments exchanged correspond to residues 1-211, 212-711 and 712-994 of SERCA1, and residues 1-264, 265-788 and 789-1159 of PMCA3 respectively. Only chimaeras containing the N-terminal segment of SERCA1 were located in the endoplasmic reticulum (ER), whereas chimaeras containing the N-terminal segment from PMCA3 were able to escape from the ER and enter the endomembrane pathway en route for the plasma membrane. Co-localization of SERCA1 in COS-7 cells with the ER/Golgi-intermediate compartment marker ERGIC53 indicates that SERCA1 is maintained in the ER by a process of retrieval. These results indicate that the N-terminal region of SERCA1, containing transmembrane helices M1 and M2, contains an ER-retrieval signal.
- Subjects :
- Animals
COS Cells
Calcium-Transporting ATPases chemistry
Cation Transport Proteins
Plasma Membrane Calcium-Transporting ATPases
Protein Binding
Sarcoplasmic Reticulum Calcium-Transporting ATPases
Subcellular Fractions metabolism
Calcium-Transporting ATPases metabolism
Endoplasmic Reticulum metabolism
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 0264-6021
- Volume :
- 371
- Issue :
- Pt 3
- Database :
- MEDLINE
- Journal :
- The Biochemical journal
- Publication Type :
- Academic Journal
- Accession number :
- 12585965
- Full Text :
- https://doi.org/10.1042/BJ20021477