IndraLab

Statements


6 | 1 6

reach
"Previously, we found that SART3 serves as a scaffold to strengthen the binding between USP15 and TUT1, and SART3 deletion mutant attenuates this binding [ 1 ]."

sparser
"Moreover, inhibition of the USP15-TUT1 cascade triggered mild and chronic endoplasmic reticulum (ER) stress."

sparser
"These findings provide a possibility that disturbance of the USP15-TUT1 cascade may induce chronic and mild ER stress, leading to an acceleration of neurodegenerative phenotype."

No evidence text available

No evidence text available

sparser
"Because the USP15-TUT1 axis is crucial for regulating U6-snRNA stabilization [ 1 ], we speculated that USP4 regulates TUT1 via deubiquitination, as does USP15 ( Fig. 2 B)."

sparser
"We presumed that SART3 regulates the binding of USP4 with TUT1 similar to the USP15-TUT1 interaction."

No evidence text available

sparser
"Because this mutant also suppresses the interaction of USP15 with TUT1 [ 1 ], we assumed that overexpression of SART3 affects endogenous USP15 rather than USP4."

No evidence text available

No evidence text available

sparser
"Intriguingly, unlike in the case of USP15-TUT1, we did not observe a strong binding between USP4 and TUT1 in the presence of SART3."

No evidence text available