XBP1 mRNA Is Induced by ATF6 and Spliced by IRE1 in Response to ER Stress to Produce a Highly Active Transcription Factor

XBP1 mRNA Is Induced by ATF6 and Spliced by IRE1 in Response to ER Stress to Produce a Highly Active Transcription Factor

I tiakina i:

Ngā taipitopito rārangi puna kōrero
Ngā kaituhi matua:	Hiderou Yoshida, Toshie Matsui, Akira Yamamoto, Tetsuya Okada, Kazutoshi Mori
Hōputu:	Artigo
Reo:	Ingarihi
I whakaputaina:	2001
Urunga tuihono:	https://doi.org/10.1016/s0092-8674(01)00611-0 https://www.cell.com/article/S0092867401006110/pdf
Ngā Tūtohu:	Tāpirihia he Tūtohu Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!

Ngā tūemi rite

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IRE1-mediated unconventional mRNA splicing and S2P-mediated ATF6 cleavage merge to regulate XBP1 in signaling the unfolded protein response
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IRE1-mediated unconventional mRNA splicing and S2P-mediated ATF6 cleavage merge to regulate XBP1 in signaling the unfolded protein response
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pXBP1(U), a Negative Regulator of the Unfolded Protein Response Activator pXBP1(S), Targets ATF6 but not ATF4 in Proteasome-mediated Degradation
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xbp-1 mRNA splicing is attenuated under prolonged exposure to ER stress
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ATF6 Activated by Proteolysis Binds in the Presence of NF-Y (CBF) Directly to the cis-Acting Element Responsible for the Mammalian Unfolded Protein Response
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ZIKV infection activates the IRE1-XBP1 and ATF6 pathways of unfolded protein response in neural cells
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ZIKV infection activates the IRE1-XBP1 and ATF6 pathways of unfolded protein response in neural cells
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Ire1 Has Distinct Catalytic Mechanisms for XBP1/HAC1 Splicing and RIDD
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Intersection of the ATF6 and XBP1 ER stress pathways in mouse islet cells
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Intersection of the ATF6 and XBP1 ER stress pathways in mouse islet cells
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Cytoplasmic IRE1α-mediated XBP1 mRNA Splicing in the Absence of Nuclear Processing and Endoplasmic Reticulum Stress
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ATF6 Activated by Proteolysis Binds in the Presence of NF-Y (CBF) Directly to the<i>cis</i>-Acting Element Responsible for the Mammalian Unfolded Protein Response
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Inhibition of ER stress–associated IRE-1/XBP-1 pathway reduces leukemic cell survival
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ERβ decreases breast cancer cell survival by regulating the IRE1/XBP-1 pathway
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XBP1
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