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פותח על ידי קלירמאש פתרונות בע"מ -
Addressing mRNAs to the ER: cis sequences act up!
Year:
2010
Source of publication :
Trends in Biochemical Sciences
Authors :
קראוט-כהן, יהודית
;
.
Volume :
35
Co-Authors:
Kraut-Cohen, J., Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel
Gerst, J.E., Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel
Facilitators :
From page:
459
To page:
469
(
Total pages:
11
)
Abstract:
Translation-coupled protein translocation requires that mRNAs encoding secreted and membrane proteins (mSMPs) reach the ER membrane. The classical view is that the signal recognition particle (SRP) pathway delivers translating signal sequence-containing proteins to the SRP receptor present on the ER surface and engages the translocation machinery. However, recent studies demonstrate both SRP- and translation-independent mRNA recruitment to the ER, and that mRNAs encoding non-signal sequence-containing cytosolic proteins (mCPs) might be full-time residents of ER membranes. Furthermore, translation-independent cis-acting sequence elements present in both mCPs and mSMPs appear to govern the ability of mRNAs to associate with ER. Thus, a more complex picture of how and why mRNAs target the ER is emerging. © 2010 Elsevier Ltd.
Note:
Related Files :
Animals
genetic analysis
Models, Biological
protein localization
protein targeting
Review
unclassified drug
עוד תגיות
תוכן קשור
More details
DOI :
10.1016/j.tibs.2010.02.006
Article number:
Affiliations:
Database:
סקופוס
Publication Type:
סקירה
;
.
Language:
אנגלית
Editors' remarks:
ID:
23040
Last updated date:
02/03/2022 17:27
Creation date:
16/04/2018 23:56
You may also be interested in
Scientific Publication
Addressing mRNAs to the ER: cis sequences act up!
35
Kraut-Cohen, J., Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel
Gerst, J.E., Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel
Addressing mRNAs to the ER: cis sequences act up!
Translation-coupled protein translocation requires that mRNAs encoding secreted and membrane proteins (mSMPs) reach the ER membrane. The classical view is that the signal recognition particle (SRP) pathway delivers translating signal sequence-containing proteins to the SRP receptor present on the ER surface and engages the translocation machinery. However, recent studies demonstrate both SRP- and translation-independent mRNA recruitment to the ER, and that mRNAs encoding non-signal sequence-containing cytosolic proteins (mCPs) might be full-time residents of ER membranes. Furthermore, translation-independent cis-acting sequence elements present in both mCPs and mSMPs appear to govern the ability of mRNAs to associate with ER. Thus, a more complex picture of how and why mRNAs target the ER is emerging. © 2010 Elsevier Ltd.
Scientific Publication
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