Modulation of chromatin modifying factors' gene expression in embryonic and induced pluripotent stem cells
Embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) are a promising source of cells for regenerative medicine because of their potential of self renew and differentiation. Multiple evidences highlight the relationship of chromatin remodeling with stem cell properties, differentiat...
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2011
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| Acceso en línea: | Registro en Scopus DOI Handle Registro en la Biblioteca Digital |
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| LEADER | 13617caa a22013937a 4500 | ||
|---|---|---|---|
| 001 | PAPER-10450 | ||
| 003 | AR-BaUEN | ||
| 005 | 20230518204029.0 | ||
| 008 | 190411s2011 xx ||||fo|||| 00| 0 eng|d | ||
| 024 | 7 | |2 scopus |a 2-s2.0-79960333291 | |
| 024 | 7 | |2 cas |a histone deacetylase, 9076-57-7; Chromatin; Transcription Factors | |
| 040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
| 030 | |a BBRCA | ||
| 100 | 1 | |a Luzzani, C. | |
| 245 | 1 | 0 | |a Modulation of chromatin modifying factors' gene expression in embryonic and induced pluripotent stem cells |
| 260 | |c 2011 | ||
| 270 | 1 | 0 | |m Guberman, A.; Laboratorio de Regulación de la Expresión Génica en el Crecimiento, Supervivencia y Diferenciación Celular Dept. de Química Biológica, Ciudad Univ., Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Intendente Guiraldes 2160, Pab. 2, 4to piso, QB-71 (C1428EGA), Buenos Aires, Argentina; email: algub@qb.fcen.uba.ar |
| 506 | |2 openaire |e Política editorial | ||
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| 504 | |a Bruggeman, S.W., Valk-Lingbeek, M.E., van der Stoop, P.P., Jacobs, J.J., Kieboom, K., Tanger, E., Hulsman, D., van Lohuizen, M., Ink4a and Arf differentially affect cell proliferation and neural stem cell self-renewal in Bmi1-deficient mice (2005) Genes Dev., 19, pp. 1438-1443 | ||
| 504 | |a Jacobs, J.J., Kieboom, K., Marino, S., DePinho, R.A., van Lohuizen, M., The oncogene and Polycomb-group gene bmi-1 regulates cell proliferation and senescence through the ink4a locus (1999) Nature, 397, pp. 164-168 | ||
| 504 | |a van der Lugt, N.M., Domen, J., Linders, K., van Roon, M., Robanus-Maandag, E., te Riele, H., van der Valk, M., van Lohuizen, M., Posterior transformation, neurological abnormalities, and severe hematopoietic defects in mice with a targeted deletion of the bmi-1 proto-oncogene (1994) Genes Dev., 8, pp. 757-769 | ||
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| 520 | 3 | |a Embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) are a promising source of cells for regenerative medicine because of their potential of self renew and differentiation. Multiple evidences highlight the relationship of chromatin remodeling with stem cell properties, differentiation programs and reprogramming for iPSC obtention.With the purpose of finding chromatin modifying factors relevant to these processes, and based on ChIP on chip studies, we selected several genes that could be modulated by Oct4, Sox2 and Nanog, critical transcription factors in stem cells, and studied their expression profile along the differentiation in mouse and human ESCs, and in mouse iPSCs. In this work, we analyzed the expression of Gcn5l2, GTF3C3, TAF15, ATF7IP, Myst2, HDAC2, HDAC3, HDAC5, HDAC10, SUV39H2, Jarid2, and Bmi-1. We found some genes from different functional groups that were highly modulated, suggesting that they could be relevant both in the undifferentiated state and during differentiation. These findings could contribute to the comprehension of molecular mechanisms involved in pluripotency, early differentiation and reprogramming. We believe that a deeper knowledge of the epigenetic regulation of ESC will allow improving somatic cell reprogramming for iPSC obtention and differentiation protocols optimization. © 2011 Elsevier Inc. |l eng | |
| 536 | |a Detalles de la financiación: Universidad de Buenos Aires, X849 | ||
| 536 | |a Detalles de la financiación: National Science and Technology Development Agency | ||
| 536 | |a Detalles de la financiación: National Council for Scientific Research | ||
| 536 | |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica, PID 115-PAE 37075 | ||
| 536 | |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas, PIP 112-200801-03003 | ||
| 536 | |a Detalles de la financiación: The authors wish to thank Estefania Rojas and Marcelo Schultz for teratoma processing. This work was supported by grants (to A.G.) from the University of Buenos Aires (X849), National Scientific and Technical Research Council (CONICET, PIP 112-200801-03003), National Agency for Science and Technology Promotion (ANPCyT, PID 115-PAE 37075) and by Biosidus S.A. C.L., C.S. and L.R. are fellows from CONICET, N.L. is supported by a fellowship grant from University of Buenos Aires and C.B. by a fellowship grant from ANPCyT. Appendix A | ||
| 593 | |a Lab. de Regulacion de la Expresion Genica en el Crecimiento, Supervivencia y Diferenciacion Celular, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Buenos Aires, Argentina | ||
| 593 | |a Laboratorio de Biología del Desarrollo Celular, Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia (FLENI), Argentina | ||
| 593 | |a Departamento de Fisiología y Biología Molecular y Celular, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina | ||
| 690 | 1 | 0 | |a CHROMATIN MODIFYING FACTORS |
| 690 | 1 | 0 | |a DIFFERENTIATION |
| 690 | 1 | 0 | |a EMBRYONIC STEM CELLS |
| 690 | 1 | 0 | |a INDUCED PLURIPOTENT STEM CELLS |
| 690 | 1 | 0 | |a BMI1 PROTEIN |
| 690 | 1 | 0 | |a CELL PROTEIN |
| 690 | 1 | 0 | |a HISTONE DEACETYLASE |
| 690 | 1 | 0 | |a HISTONE DEACETYLASE 10 |
| 690 | 1 | 0 | |a HISTONE DEACETYLASE 2 |
| 690 | 1 | 0 | |a HISTONE DEACETYLASE 3 |
| 690 | 1 | 0 | |a HISTONE DEACETYLASE 5 |
| 690 | 1 | 0 | |a PROTEIN ATF7IP |
| 690 | 1 | 0 | |a PROTEIN GCN512 |
| 690 | 1 | 0 | |a PROTEIN GTF3C3 |
| 690 | 1 | 0 | |a PROTEIN JARID2 |
| 690 | 1 | 0 | |a PROTEIN MYST2 |
| 690 | 1 | 0 | |a PROTEIN SUV39H2 |
| 690 | 1 | 0 | |a PROTEIN TAF15 |
| 690 | 1 | 0 | |a UNCLASSIFIED DRUG |
| 690 | 1 | 0 | |a ANIMAL CELL |
| 690 | 1 | 0 | |a ARTICLE |
| 690 | 1 | 0 | |a CELL DIFFERENTIATION |
| 690 | 1 | 0 | |a CHROMATIN ASSEMBLY AND DISASSEMBLY |
| 690 | 1 | 0 | |a EMBRYONIC STEM CELL |
| 690 | 1 | 0 | |a GENE EXPRESSION |
| 690 | 1 | 0 | |a HUMAN |
| 690 | 1 | 0 | |a HUMAN CELL |
| 690 | 1 | 0 | |a MOUSE |
| 690 | 1 | 0 | |a NONHUMAN |
| 690 | 1 | 0 | |a PLURIPOTENT STEM CELL |
| 690 | 1 | 0 | |a PRIORITY JOURNAL |
| 690 | 1 | 0 | |a PROTEIN EXPRESSION |
| 690 | 1 | 0 | |a ANIMALS |
| 690 | 1 | 0 | |a CELL LINE |
| 690 | 1 | 0 | |a CHROMATIN |
| 690 | 1 | 0 | |a CHROMATIN IMMUNOPRECIPITATION |
| 690 | 1 | 0 | |a EMBRYONIC STEM CELLS |
| 690 | 1 | 0 | |a GENE EXPRESSION REGULATION |
| 690 | 1 | 0 | |a HUMANS |
| 690 | 1 | 0 | |a INDUCED PLURIPOTENT STEM CELLS |
| 690 | 1 | 0 | |a MICE |
| 690 | 1 | 0 | |a TRANSCRIPTION FACTORS |
| 700 | 1 | |a Solari, C. | |
| 700 | 1 | |a Losino, N. | |
| 700 | 1 | |a Ariel, W. | |
| 700 | 1 | |a Romorini, L. | |
| 700 | 1 | |a Bluguermann, C. | |
| 700 | 1 | |a Sevlever, G. | |
| 700 | 1 | |a Barañao, L. | |
| 700 | 1 | |a Miriuka, S. | |
| 700 | 1 | |a Guberman, A. | |
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