Subbareddy Maddika
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COP9 signalosome and PRMT5 methylosome complexes are essential regulators of Lis1-dynein based transport
Abstract Cytoplasmic dynein is a minus-end directed microtubule motor essential for retrograde transport in cells. Dynein is tightly regulated by Lis1 where it is reported to stall dynein movement as well as promote formation of active dynein in different model systems. However, the mechanism behind these contrasting functions of Lis1 in regulating dynein is unknown. Here, we identified COP9 Signalosome (CSN) and PRMT5 complexes as critical regulators of Lis1 dependent dynein function.
Ubiquitin‐independent proteasomal degradation of Spindlin‐1 by the E3 ligase HACE1 contributes to cell-cell adhesion
Research Article Subbareddy Maddika Corresponding Author msreddy@cdfd.org.in orcid.org/0000-0002-5880-391X Laboratory of Cell Death & Cell Survival, Centre for DNA Fingerprinting and Diagnostics (CDFD), Uppal, India Correspondence S.
PTEN Regulates Glucose Transporter Recycling by Impairing SNX27 Retromer Assembly
Measurement of GLUT1 Levels at the Plasma Membrane In conclusion, our data clearly demonstrate that PTEN binds with SNX27, hinders its access to the VPS26 retromer complex, and prevents the recycling of GLUT1 to the plasma membrane, followed by impaired glucose uptake (shown in the model in Figure 6Figure 6G). A recent study (Garcia-Cao et al., 2012xSystemic elevation of PTEN induces a tumor-suppressive metabolic state.
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