siRNA screen of the human signaling proteome identifies the PtdIns(3,4,5)P3-mTOR signaling pathway as a primary regulator of transferrin uptake 英文参考文献.docVIP
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siRNA screen of the human signaling proteome identifies the PtdIns(3,4,5)P3-mTOR signaling pathway as a primary regulator of transferrin uptake 英文参考文献
Open Access
Re rch
2007GalvezetVoal.umesea8, Issue 7, Article R142
siRNA screen of the human signaling proteome identifies the
PtdIns(3,4,5)P3-mTOR signaling pathway as a primary regulator of
transferrin uptake
Thierry Galvez, Mary N Teruel, Won Do Heo, Joshua T Jones,
Man Lyang Kim, Jen Liou, Jason W Myers and Tobias Meyer
Address: Department of Chemical and Systems Biology and Bio-X Program, Stanford University School of Medicine, Stanford, CA 94305, USA.
Correspondence: Thierry Galvez. Email: galvez@mpi-cbg.de. Tobias Meyer. Email: tobias1@
Published: 19 July 2007
Received: 16 February 2007
Revised: 30 May 2007
Accepted: 19 July 2007
Genome Biology 2007, 8:R142 (doi:10.1186/gb-2007-8-7-r142)
The electronic version of this article is the complete one and can be
found online at /2007/8/7/R142
? 2007 Galvez et al.; licensee BioMed Central Ltd.
This is an open access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0), which
permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Regulators3,p4,5A-tsruisrpvheofyosotransferrinpfh1a,8te0-4mhTuOmuptakeRansigdicer-generatednaling pathwaysignalingas a primsiRNAsary reguusinglator oautomatedf iron-tranquantitativesferrin uptakimaginge./p identified the phosphatidylinositol-
Abstract
Background: Iron uptake via endocytosis of iron-transferrin-transferrin receptor complexes is a
rate-limiting step for cell growth, viability and proliferation in tumor cells as well as non-
transformed cells such as activated lymphocytes. Signaling pathways that regulate transferrin uptake
have not yet been identified.
Results: We surveyed the human signaling proteome for regulators that increase or decrease
transferrin uptake by screening 1,804 dicer-generated signaling small interfering RNAs using
automated quantitative imaging. In addition to known transport proteins, we id
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