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Cytoplasmic retention signals

Pines J, Hunter T. 1994. The differential localization of human cyclins A and B is due to a cytoplasmic retention signal in cyclin B. EMBO J 13 3772-3781. [Pg.234]

Because proteins are synthesized within the cytosol (including on the surface of the ER), it is plausible to postulate that the localization at the cytosol is a default. Such a notion is challenged by the discoveries of several cytoplasmic targeting/retention signals. In one example, the N-terminal 42 residue segment of cyclin B directs it to the cytosol if it is deleted, it is transported to the nucleus and the addition of the segment to cyclin A causes its cytosolic retention (Pines and Hunter,... [Pg.328]

Kanno, Y., Suzuki, M., Nakahama, T., and Inouye, Y. (2005) Characterization of nuclear localization signals and cytoplasmic retention region in the nuclear receptor CAR. Biochim. Biophys. Acta 1745, 215-222. [Pg.178]

Nilsson, T., Jackson, M., and Pederson, P. A. (1989). Short cytoplasmic sequences serve as retention signals for transmembrane proteins in the endoplasmic reticulum. Cell 58, 707-718. [Pg.40]

In addition to the membrane-inserted core domain of Kv channels, their cytoplasmic domains have important roles for Kv-channel function [5]. Many of these functions are related to subunits assembly, channel trafficking to and from the plasma membrane, and interactions with cytoskeletal components (Fig. la). A tetramerization (T) domain for subunit assembly has been well defined in Shaker-channels, where it is localized in the amino-terminus. Other Kv-channels (e.g., eag, HERG, KvLQTl) may have comparable domains within the cytoplasmic carboxy-terminus. ER retention and retrieval signals have been found... [Pg.1309]


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