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  1. Article ; Online: Alteration of the transcriptional profile of human embryonic kidney cells by transient overexpression of mouse TRPM7 channels.

    Lee, Byoung-Cheol / Hong, Seong-Eui / Lim, Hyun-Ho / Kim, Do Han / Park, Chul-Seung

    Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology

    2011  Volume 27, Issue 3-4, Page(s) 313–326

    Abstract: ... on cellular gene expression, inducible HEK293 cell-lines harboring the wild-type mouse TRPM7 and a mutant ... lacking the kinase domain were established. The wild-type and the non-functional TRPM7 channels were ... in transcription significantly and specifically by the expression of the functional TRPM7 channel.: Conclusion ...

    Abstract Background: TRPM7 is a cation channel containing a functional kinase domain. The functional activity of TRPM7 is essential for cell viability and growth, and its expression is up-regulated in certain pathological conditions, such as ischemia.
    Methods: In order to assess the effects of TRPM7 activity on cellular gene expression, inducible HEK293 cell-lines harboring the wild-type mouse TRPM7 and a mutant lacking the kinase domain were established. The wild-type and the non-functional TRPM7 channels were induced transiently and the comparative changes in cellular transcription were investigated.
    Results: From the genome-scale analysis using a human genome expression microarray, we identified 951 genes altered in transcription significantly and specifically by the expression of the functional TRPM7 channel.
    Conclusion: By analyzing the genes differentially expressed by TRPM7, we were able to provide potential target proteins and to delineate the cellular pathways affected by the channel function.
    MeSH term(s) Animals ; Gene Expression Profiling ; Genome, Human ; HEK293 Cells ; Humans ; Mice ; Microarray Analysis ; TRPM Cation Channels/genetics ; TRPM Cation Channels/metabolism ; Transfection
    Chemical Substances TRPM Cation Channels ; Trpm7 protein, mouse (EC 2.7.1.-)
    Language English
    Publishing date 2011-04-01
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1067572-3
    ISSN 1421-9778 ; 1015-8987
    ISSN (online) 1421-9778
    ISSN 1015-8987
    DOI 10.1159/000327958
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Alteration of the Transcriptional Profile of Human Embryonic Kidney Cells by Transient Overexpression of Mouse TRPM7 Channels

    Lee, Byoung-Cheol / Hong, Seong-Eui / Lim, Hyun-Ho / Kim, Do Han / Park, Chul-Seung

    Cellular Physiology and Biochemistry - International Journal of Experimental Cellular Physiology, Biochemistry andPharmacology

    2011  Volume 27, Issue 3_4, Page(s) 313–326

    Abstract: ... on cellular gene expression, inducible HEK293 cell-lines harboring the wild-type mouse TRPM7 and a mutant ... lacking the kinase domain were established. The wild-type and the non-functional TRPM7 channels were ... in transcription significantly and specifically by the expression of the functional TRPM7 channel. Conclusion ...

    Abstract Background: TRPM7 is a cation channel containing a functional kinase domain. The functional activity of TRPM7 is essential for cell viability and growth, and its expression is up-regulated in certain pathological conditions, such as ischemia. Methods: In order to assess the effects of TRPM7 activity on cellular gene expression, inducible HEK293 cell-lines harboring the wild-type mouse TRPM7 and a mutant lacking the kinase domain were established. The wild-type and the non-functional TRPM7 channels were induced transiently and the comparative changes in cellular transcription were investigated. Results: From the genome-scale analysis using a human genome expression microarray, we identified 951 genes altered in transcription significantly and specifically by the expression of the functional TRPM7 channel. Conclusion: By analyzing the genes differentially expressed by TRPM7, we were able to provide potential target proteins and to delineate the cellular pathways affected by the channel function.
    Keywords TRPM7 ; Microarray ; Transcriptome ; Differential Expression ; Cellular Pathway
    Language English
    Publisher S. Karger AG
    Publishing place Basel
    Publishing country Switzerland
    Document type Article ; Online
    ISSN 1421-9778 ; 1015-8987 ; 1015-8987
    ISSN (online) 1421-9778
    ISSN 1015-8987
    DOI 10.1159/000327958
    Database Karger publisher's database

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  3. Article: Alteration of the Transcriptional Profile of Human Embryonic Kidney Cells by Transient Overexpression of Mouse TRPM7 Channels

    Lee, Byoung-Cheol / Hong, Seong-Eui / Lim, Hyun-Ho / Kim, Do Han / Park, Chul-Seung

    Cellular Physiology and Biochemistry

    2011  Volume 27, Issue 3-4, Page(s) 313–326

    Abstract: ... on cellular gene expression, inducible HEK293 cell-lines harboring the wild-type mouse TRPM7 and a mutant ... lacking the kinase domain were established. The wild-type and the non-functional TRPM7 channels were ... in transcription significantly and specifically by the expression of the functional TRPM7 channel. Conclusion ...

    Institution School of Life Sciences Systems Biology Research Center Center for Distributed Sensor Network Cell Dynamics Research Center, Gwangju Institute of Science and Technology (GIST), Gwangju
    Abstract Background: TRPM7 is a cation channel containing a functional kinase domain. The functional activity of TRPM7 is essential for cell viability and growth, and its expression is up-regulated in certain pathological conditions, such as ischemia. Methods: In order to assess the effects of TRPM7 activity on cellular gene expression, inducible HEK293 cell-lines harboring the wild-type mouse TRPM7 and a mutant lacking the kinase domain were established. The wild-type and the non-functional TRPM7 channels were induced transiently and the comparative changes in cellular transcription were investigated. Results: From the genome-scale analysis using a human genome expression microarray, we identified 951 genes altered in transcription significantly and specifically by the expression of the functional TRPM7 channel. Conclusion: By analyzing the genes differentially expressed by TRPM7, we were able to provide potential target proteins and to delineate the cellular pathways affected by the channel function.
    Keywords TRPM7 ; Microarray ; Transcriptome ; Differential Expression ; Cellular Pathway
    Language English
    Publishing date 2011-04-01
    Publisher S. Karger AG
    Publishing place Basel, Switzerland
    Document type Article
    Note Original Paper
    ZDB-ID 1067572-3
    ISSN 1421-9778 ; 1015-8987
    ISSN (online) 1421-9778
    ISSN 1015-8987
    DOI 10.1159/000327958
    Database Karger publisher's database

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