PinX1t, a Novel PinX1 Transcript Variant, Positively Regulates Cardiogenesis of Embryonic Stem Cells.

Background Pin2/TRF1-interacting protein, PinX1, was previously identified as a tumor suppressor. Here, we discovered a novel transcript variant of mPinX1 (mouse PinX1), mPinX1t (mouse PinX1t), in embryonic stem cells (ESCs). The aims of this investigation were (1) to detect the presence of mPinX1 a...

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Publicado en:Journal of the American Heart Association Vol. 9; no. 6; pp. 1 - 56
Autores principales: Hing Chung Chan, Yuen Ting Lau, Qianqian Ding, Chun Kit Li, Chi Ming Wong, Pang Chui Shaw, Mary Miu Yee Waye, Suk Ying Tsang, Chan, Hing Chung, Lau, Yuen Ting, Ding, Qianqian, Li, Chun Kit, Wong, Chi Ming, Shaw, Pang Chui, Waye, Mary Miu Yee, Tsang, Suk Ying
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 3/17/2020
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 3/17/2020
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        10.1161/JAHA.118.010240
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        atl: PinX1t, a Novel PinX1 Transcript Variant, Positively Regulates Cardiogenesis of Embryonic Stem Cells.
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        au:
          Hing Chung Chan
          Yuen Ting Lau
          Qianqian Ding
          Chun Kit Li
          Chi Ming Wong
          Pang Chui Shaw
          Mary Miu Yee Waye
          Suk Ying Tsang
          Chan, Hing Chung
          Lau, Yuen Ting
          Ding, Qianqian
          Li, Chun Kit
          Wong, Chi Ming
          Shaw, Pang Chui
          Waye, Mary Miu Yee
          Tsang, Suk Ying
        affil: School of Life Sciences, Hong Kong SAR
      sug:
        subj:
          Cell Differentiation
          Proteins Metabolism
          Cell Cycle Proteins Metabolism
          Cells Metabolism
          Carrier Proteins
          Morphogenesis
          Carrier Proteins Metabolism
          Transcription Factors
          Animal Studies
          Genes
          Histocompatibility Antigens
          RNA Metabolism
          Transcription Factors Metabolism
          RNA
          Cell Line
          Proteins
          Signal Transduction
          Mice
          Histocompatibility Antigens Metabolism
          Cell Cycle Proteins
          Comparative Studies
          Multicenter Studies
          Evaluation Research
          Validation Studies
      ab: Background Pin2/TRF1-interacting protein, PinX1, was previously identified as a tumor suppressor. Here, we discovered a novel transcript variant of mPinX1 (mouse PinX1), mPinX1t (mouse PinX1t), in embryonic stem cells (ESCs). The aims of this investigation were (1) to detect the presence of mPinX1 and mPinX1t in ESCs and their differentiation derivatives; (2) to investigate the role of mPinX1 and mPinX1t on regulating the characteristics of undifferentiated ESCs and the cardiac differentiation of ESCs; (3) to elucidate the molecular mechanisms of how mPinX1 and mPinX1t regulate the cardiac differentiation of ESCs. Methods and Results By 5' rapid amplification of cDNA ends, 3' rapid amplification of cDNA ends, and polysome fractionation followed by reverse transcription-polymerase chain reaction, mPinX1t transcript was confirmed to be an intact mRNA that is actively translated. Western blot confirmed the existence of mPinX1t protein. Overexpression or knockdown of mPinX1 (both decreased mPinX1t expression) both decreased while overexpression of mPinX1t increased the cardiac differentiation of ESCs. Although both mPinX1 and mPinX1t proteins were found to bind to cardiac transcription factor mRNAs, only mPinX1t protein but not mPinX1 protein was found to bind to nucleoporin 133 protein, a nuclear pore complex component. In addition, mPinX1t-containing cells were found to have a higher cytosol-to-nucleus ratio of cardiac transcription factor mRNAs when compared with that in the control cells. Our data suggested that mPinX1t may positively regulate cardiac differentiation by enhancing export of cardiac transcription factor mRNAs through interacting with nucleoporin 133. Conclusions We discovered a novel transcript variant of mPinX1, the mPinX1t, which positively regulates the cardiac differentiation of ESCs.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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