GATA gene transcriptions: Difference between revisions
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SRF is important during the development of the embryo, as it has been linked to the formation of mesoderm.<ref name="pmid11983708">{{cite journal | vauthors = Sepulveda JL, Vlahopoulos S, Iyer D, Belaguli N, Schwartz RJ | title = Combinatorial expression of GATA4, Nkx2-5, and serum response factor directs early cardiac gene activity | journal = J. Biol. Chem. | volume = 277 | issue = 28 | pages = 25775–82 | date = July 2002 | pmid = 11983708 | doi = 10.1074/jbc.M203122200 }}</ref><ref name="pmid15591049">{{cite journal | vauthors = Barron MR, Belaguli NS, Zhang SX, Trinh M, Iyer D, Merlo X, Lough JW, Parmacek MS, Bruneau BG, Schwartz RJ | title = Serum response factor, an enriched cardiac mesoderm obligatory factor, is a downstream gene target for Tbx genes | journal = J. Biol. Chem. | volume = 280 | issue = 12 | pages = 11816–28 | date = March 2005 | pmid = 15591049 | doi = 10.1074/jbc.M412408200 }}</ref> | [[SRF]] is important during the development of the embryo, as it has been linked to the formation of mesoderm.<ref name="pmid11983708">{{cite journal | vauthors = Sepulveda JL, Vlahopoulos S, Iyer D, Belaguli N, Schwartz RJ | title = Combinatorial expression of GATA4, Nkx2-5, and serum response factor directs early cardiac gene activity | journal = J. Biol. Chem. | volume = 277 | issue = 28 | pages = 25775–82 | date = July 2002 | pmid = 11983708 | doi = 10.1074/jbc.M203122200 }}</ref><ref name="pmid15591049">{{cite journal | vauthors = Barron MR, Belaguli NS, Zhang SX, Trinh M, Iyer D, Merlo X, Lough JW, Parmacek MS, Bruneau BG, Schwartz RJ | title = Serum response factor, an enriched cardiac mesoderm obligatory factor, is a downstream gene target for Tbx genes | journal = J. Biol. Chem. | volume = 280 | issue = 12 | pages = 11816–28 | date = March 2005 | pmid = 15591049 | doi = 10.1074/jbc.M412408200 }}</ref> | ||
The Serum response factor (SRF) has been shown to interact with GATA4.<ref name = pmid11003651>{{cite journal | vauthors = Belaguli NS, Sepulveda JL, Nigam V, Charron F, Nemer M, Schwartz RJ | title = Cardiac tissue enriched factors serum response factor and GATA-4 are mutual coregulators | journal = Mol. Cell. Biol. | volume = 20 | issue = 20 | pages = 7550–8 | date = October 2000 | pmid = 11003651 | pmc = 86307 | doi = 10.1128/mcb.20.20.7550-7558.2000}}</ref><ref name = pmid11158291>{{cite journal | vauthors = Morin S, Paradis P, Aries A, Nemer M | title = Serum response factor-GATA ternary complex required for nuclear signaling by a G-protein-coupled receptor | journal = Mol. Cell. Biol. | volume = 21 | issue = 4 | pages = 1036–44 | date = February 2001 | pmid = 11158291 | pmc = 99558 | doi = 10.1128/MCB.21.4.1036-1044.2001 }}</ref> | The Serum response factor (SRF) has been shown to interact with [[GATA4]].<ref name = pmid11003651>{{cite journal | vauthors = Belaguli NS, Sepulveda JL, Nigam V, Charron F, Nemer M, Schwartz RJ | title = Cardiac tissue enriched factors serum response factor and GATA-4 are mutual coregulators | journal = Mol. Cell. Biol. | volume = 20 | issue = 20 | pages = 7550–8 | date = October 2000 | pmid = 11003651 | pmc = 86307 | doi = 10.1128/mcb.20.20.7550-7558.2000}}</ref><ref name = pmid11158291>{{cite journal | vauthors = Morin S, Paradis P, Aries A, Nemer M | title = Serum response factor-GATA ternary complex required for nuclear signaling by a G-protein-coupled receptor | journal = Mol. Cell. Biol. | volume = 21 | issue = 4 | pages = 1036–44 | date = February 2001 | pmid = 11158291 | pmc = 99558 | doi = 10.1128/MCB.21.4.1036-1044.2001 }}</ref> | ||
Cell specific developmental expression is tightly controlled, but, once expressed, require no additional activation -- GATA transcription factor (GATA), hepatocyte nuclear factors (HNF), PIT-1, MyoD, Myf5, Hox, winged-helix transcription factors. | Cell specific developmental expression is tightly controlled, but, once expressed, require no additional activation -- [[GATA transcription factor]] ([[GATA]]), [[hepatocyte nuclear factors]] ([[HNF]]), [[PIT-1]], [[MyoD]], [[Myf5]], [[Hox]], winged-helix transcription factors. | ||
The class of diverse Cys4 zinc fingers includes the family of GATA-factors. | The class of diverse [[Cys4]] zinc fingers includes the family of GATA-factors. | ||
In the diagram on the right, STAT5 may be involved with an erythropoiesis receptor, or Epo Receptor. Murine, members of the subfamily '''Murinae''', Epo Receptor truncations and known functions are included. Erythroid differentiation depends on transcriptional regulator GATA1, zinc finger DNA binding domain binds specifically to DNA consensus sequence [AT]GATA[AG] promoter elements. In erythropoiesis, EpoR is best known for inducing survival of progenitors. | In the diagram on the right, [[STAT5]] may be involved with an erythropoiesis receptor, or [[Epo Receptor]]. Murine, members of the subfamily '''Murinae''', Epo Receptor truncations and known functions are included. Erythroid differentiation depends on transcriptional regulator [[GATA1]], zinc finger DNA binding domain binds specifically to DNA consensus sequence [AT]GATA[AG] promoter elements. In erythropoiesis, EpoR is best known for inducing survival of progenitors. | ||
Some "putative wound-response elements including AGC box-like sequences<sup>28</sup>, TCA motif-like sequences<sup>28</sup>, carrot extensin gene wound-response elements (AT-rich motif, TTTTTTT, TGACGT)<sup>29</sup>, constitutive PAL footprint and elicitor-inducible PAL footprint<sup>31</sup>, and proteinase inhibitor II footprint<sup>31</sup> have been found in cabch29 promoter. Some cis-elements related to organ and tissue-specific expression such as GATA motif-like sequence, ASF-1 binding site-like elements also existed in 5′ upstream region. Meanwhile, some basic transcriptional regulatory cis-elements including G box-like and GC box-like elements are located in this region."<ref name=Tang>{{ cite journal | Some "putative wound-response elements including AGC box-like sequences<sup>28</sup>, TCA motif-like sequences<sup>28</sup>, carrot extensin gene wound-response elements (AT-rich motif, TTTTTTT, TGACGT)<sup>29</sup>, constitutive [[PAL]] footprint and elicitor-inducible PAL footprint<sup>31</sup>, and proteinase inhibitor II footprint<sup>31</sup> have been found in cabch29 promoter. Some cis-elements related to organ and tissue-specific expression such as [[GATA]] motif-like sequence, [[ASF-1]] binding site-like elements also existed in 5′ upstream region. Meanwhile, some basic transcriptional regulatory cis-elements including [[G box]]-like and [[GC box]]-like elements are located in this region."<ref name=Tang>{{ cite journal | ||
|author=Guo Qing Tang, Yong Yan Bai & Shi Wei Loo | |author=Guo Qing Tang, Yong Yan Bai & Shi Wei Loo | ||
|title=Functional properties of a cabbage chitinase promoter from cabbage (''Brassica oleracea var. capitata'') | |title=Functional properties of a cabbage chitinase promoter from cabbage (''Brassica oleracea var. capitata'') | ||
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|accessdate=24 March 2019 }}</ref> | |accessdate=24 March 2019 }}</ref> | ||
"A computer search for transcription promoter elements [...] showed the presence of a prominent TATA box 22 nucleotides upstream of the transcription start site and an Sp1 site at position -42 to -33. The 5'-flanking sequence also contains three E boxes with CANNTG consensus sequences at positions -464 to -459, -90 to -85, and -52 to -47 that have been marked as E box, E1 box, and E2 box, respectively [...]. In addition, the 5'-flanking region contains one or more GRE, XRE, GATA-1, GCN-4, PEA-3, AP1, and AP2 consensus motifs and also three imperfect CArG sites [...]."<ref name=Lenka>{{ cite journal | "A computer search for transcription promoter elements [...] showed the presence of a prominent TATA box 22 nucleotides upstream of the transcription start site and an [[Sp1]] site at position -42 to -33. The 5'-flanking sequence also contains three E boxes with CANNTG consensus sequences at positions -464 to -459, -90 to -85, and -52 to -47 that have been marked as [[E box]], [[E1 box]], and [[E2 box]], respectively [...]. In addition, the 5'-flanking region contains one or more [[GRE]], [[XRE]], [[GATA-1]], [[GCN-4]], [[PEA-3]], [[AP1]], and [[AP2]] consensus motifs and also three imperfect CArG sites [...]."<ref name=Lenka>{{ cite journal | ||
|author=Nibedita Lenka, Aruna Basu, Jayati Mullick, and Narayan G. Avadhani | |author=Nibedita Lenka, Aruna Basu, Jayati Mullick, and Narayan G. Avadhani | ||
|title=The role of an E box binding basic helix loop helix protein in the cardiac muscle-specific expression of the rat cytochrome oxidase subunit VIII gene | |title=The role of an E box binding basic helix loop helix protein in the cardiac muscle-specific expression of the rat cytochrome oxidase subunit VIII gene | ||
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|accessdate=7 February 2019 }}</ref> | |accessdate=7 February 2019 }}</ref> | ||
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== Single transcription factor transdifferentiation == | == Single transcription factor transdifferentiation == | ||
Brief expression of a single transcription factor, the ELT-7 GATA factor, can convert the identity of fully differentiated, specialized non-endodermal cells of the pharynx into fully differentiated intestinal cells in intact larvae and adult roundworm ''Caenorhabditis elegans'' with no requirement for a dedifferentiated intermediate.<ref name=Riddle>{{cite journal | Brief expression of a single transcription factor, the [[ELT-7]] GATA factor, can convert the identity of fully differentiated, specialized non-endodermal cells of the pharynx into fully differentiated intestinal cells in intact larvae and adult roundworm ''Caenorhabditis elegans'' with no requirement for a dedifferentiated intermediate.<ref name=Riddle>{{cite journal | ||
|author=Misty R. Riddle, Abraham Weintraub, Ken C. Q. Nguyen, David H. Hall, and Joel H. Rothman | |author=Misty R. Riddle, Abraham Weintraub, Ken C. Q. Nguyen, David H. Hall, and Joel H. Rothman | ||
|title=Transdifferentiation and remodeling of post-embryonic ''C. elegans'' cells by a single transcription factor | |title=Transdifferentiation and remodeling of post-embryonic ''C. elegans'' cells by a single transcription factor | ||
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|accessdate=29 December 2019 }}</ref> | |accessdate=29 December 2019 }}</ref> | ||
"ELT-7, a GATA transcription factor that regulates terminal intestinal differentiation (Maduro and Rothman, 2002; Sommermann et al., 2010), activates an intestinal marker (elt-2::lacZ::GFP) in non-intestinal cells when briefly ectopically expressed via a heat-shock promoter at any embryonic, larval, or adult stage [...]."<ref name=Riddle/> | "ELT-7, a GATA transcription factor that regulates terminal intestinal differentiation (Maduro and Rothman, 2002; Sommermann et al., 2010), activates an intestinal marker ([[elt-2]]::[[lacZ]]::[[GFP]]) in non-intestinal cells when briefly ectopically expressed via a heat-shock promoter at any embryonic, larval, or adult stage [...]."<ref name=Riddle/> | ||
The "END-1 GATA transcription factor, which specifies the endoderm progenitor (Zhu et al., 1997), does not activate widespread intestinal gene expression after the MCT [...]."<ref name=Riddle/> | The "[[END-1]] GATA transcription factor, which specifies the endoderm progenitor (Zhu et al., 1997), does not activate widespread intestinal gene expression after the [[MCT]] [...]."<ref name=Riddle/> | ||
== Cardiomyocytes == | == Cardiomyocytes == | ||
Cell-based ''in vivo'' therapies may provide a transformative approach to augment vascular and muscle growth and to prevent non-contractile scar formation by delivering transcription factors<ref name="Li">{{cite doi|10.1038/nature11044}}</ref> or microRNAs<ref name="Dzau">{{cite doi|10.1161/CIRCRESAHA.112.269035}}</ref> to the heart.<ref name="Chunhui">{{cite doi|10.1016/j.molmed.2012.06.009}}</ref> Cardiac fibroblasts, which represent 50% of the cells in the mammalian heart, can be reprogrammed into [[w:Cardiac muscle|cardiomyocyte]]-like cells in vivo by local delivery of cardiac core transcription factors ( GATA4, MEF2C, TBX5 and for improved reprogramming plus ESRRG, MESP1, Myocardin and ZFPM2) after coronary | Cell-based ''in vivo'' therapies may provide a transformative approach to augment vascular and muscle growth and to prevent non-contractile scar formation by delivering transcription factors<ref name="Li">{{cite doi|10.1038/nature11044}}</ref> or microRNAs<ref name="Dzau">{{cite doi|10.1161/CIRCRESAHA.112.269035}}</ref> to the heart.<ref name="Chunhui">{{cite doi|10.1016/j.molmed.2012.06.009}}</ref> Cardiac fibroblasts, which represent 50% of the cells in the mammalian heart, can be reprogrammed into [[w:Cardiac muscle|cardiomyocyte]]-like cells in vivo by local delivery of cardiac core transcription factors ([[GATA4]], [[MEF2C]], [[TBX5]] and for improved reprogramming plus [[ESRRG]], [[MESP1]], [[Myocardin]] and [[ZFPM2]]) after coronary ligation.<ref name="Li"/><ref>{{cite doi|10.1016/j.stemcr.2013.07.005}}</ref> These results implicated therapies that can directly remuscularize the heart without cell transplantation. However, the efficiency of such reprogramming turned out to be very low and the phenotype of received cardiomyocyte-like cells does not resemble those of a mature normal cardiomyocyte. Furthermore, transplantation of cardiac transcription factors into injured murine hearts resulted in poor cell survival and minimal expression of cardiac genes.<ref name="Sean">{{cite doi|10.1161/CIRCRESAHA.112.270264}}</ref> | ||
== Blood stem cells == | == Blood stem cells == | ||
Definitive hematopoiesis emerges during embryogenesis via an endothelial-to-hematopoietic transition. Combination of four transcription factors, [[GATA2]], [[GFI1B]], [[c-Fos]], and [[ETV6]], is sufficient to induce ''in vitro'' development leading to the formation of endothelial-like precursor cells, with the subsequent appearance of hematopoietic cells.<ref>Pereira, C. F., Chang, B., Qiu, J., Niu, X., Papatsenko, D., Hendry, C. E., ... & Moore, K. (2013). Induction of a hemogenic program in mouse fibroblasts. Cell stem cell, 13(2), 205-218. DOI: http://dx.doi.org/10.1016/j.stem.2013.05.024</ref> Transient expression of six transcription factors ([[RUNX1T1]], [[HLF]], [[LMO2]], [[Prdm5]], [[PBX1]], [[ZFP36]]) and also [[N-Myc]] with [[MEIS1]], to improve reprogramming efficacy, is sufficient to activate the gene networks governing hematopoietic stem cells functional identity in committed blood cells. This finding marks a significant step toward one of the most sought-after goals of regenerative medicine: the ability to produce hematopoietic stem cells suitable for transplantation, using more mature or differentiated blood cells to make up the shortfall of bone marrow transplants<ref>Jonah Riddell, Roi Gazit, Brian S. Garrison, et al., & Derrick J. Rossi (2014). Reprogramming Committed Murine Blood Cells to Induced Hematopoietic Stem Cells with Defined Factors. Cell, 157(30, 549–564, DOI: http://dx.doi.org/10.1016/j.cell.2014.04.006</ref> It should be noted, however, that the transcription factors used in this study belong to a group of proto-oncogenes and therefore these cells could be dangerous to humans. Still to be answered are the precise contribution of each of the eight factors to the reprogramming process and whether approaches that do not rely on viruses and transcription factors can have similar success. It also is not yet known whether the same results can be achieved using human cells or whether other, non-blood cells can be reprogrammed to | Definitive hematopoiesis emerges during embryogenesis via an endothelial-to-hematopoietic transition. Combination of four transcription factors, [[GATA2]], [[GFI1B]], [[c-Fos]], and [[ETV6]], is sufficient to induce ''in vitro'' development leading to the formation of endothelial-like precursor cells, with the subsequent appearance of hematopoietic cells.<ref>Pereira, C. F., Chang, B., Qiu, J., Niu, X., Papatsenko, D., Hendry, C. E., ... & Moore, K. (2013). Induction of a hemogenic program in mouse fibroblasts. Cell stem cell, 13(2), 205-218. DOI: http://dx.doi.org/10.1016/j.stem.2013.05.024</ref> Transient expression of six transcription factors ([[RUNX1T1]], [[HLF]], [[LMO2]], [[Prdm5]], [[PBX1]], [[ZFP36]]) and also [[N-Myc]] with [[MEIS1]], to improve reprogramming efficacy, is sufficient to activate the gene networks governing hematopoietic stem cells functional identity in committed blood cells. This finding marks a significant step toward one of the most sought-after goals of regenerative medicine: the ability to produce hematopoietic stem cells suitable for transplantation, using more mature or differentiated blood cells to make up the shortfall of bone marrow transplants<ref>Jonah Riddell, Roi Gazit, Brian S. Garrison, et al., & Derrick J. Rossi (2014). Reprogramming Committed Murine Blood Cells to Induced Hematopoietic Stem Cells with Defined Factors. Cell, 157(30, 549–564, DOI: http://dx.doi.org/10.1016/j.cell.2014.04.006</ref> It should be noted, however, that the transcription factors used in this study belong to a group of proto-oncogenes and therefore these cells could be dangerous to humans. Still to be answered are the precise contribution of each of the eight factors to the reprogramming process and whether approaches that do not rely on viruses and transcription factors can have similar success. It also is not yet known whether the same results can be achieved using human cells or whether other, non-blood cells can be reprogrammed to [[iHSC]]s.<ref>Boston Children's Hospital."[http://www.sciencedaily.com/releases/2014/04/140424125239.htm?utm_source=feedburner Blood cells reprogrammed into blood stem cells in mice]". ScienceDaily, 24 April 2014</ref> | ||
==See also== | ==See also== | ||
Revision as of 17:37, 30 December 2019
Associate Editor(s)-in-Chief: Henry A. Hoff
Although "the P3, P6 substitutions alter the conserved 'GATAAG' I box motif, a 'GATA' motif is present in the introduced EcoRV site. This introduced GATA sequence clearly does not serve as a functional I box [...]."[1]
"The I-box motif, 5'-GGATGAGATAAGA-3', or its shorter version 5'-GATAAG-3', has been found in the promoters of a large number of RBCS genes (Giuliano et al., 1988; Manzara and Gruissem, 1988). A related motif (the GATA box) is present in the promoters of the light-regulated chlorophyll a/b binding protein (CAB) genes of different species (Gidoni et al., 1989), and has been shown to be involved in the activation of an Arabidopsis CAB gene by light and by the circadian clock (Anderson and Kay, 1995). I-box and GATA binding factors have been identified in nuclear extracts from tobacco and tomato leaves and cotyledons (Borello et al., 1993; Giuliano et al., 1988; Manzara et al., 1991; Schindler and Cashmore, 1990). The I-box has therefore been suggested to be involved in light-regulated and/or leaf-specific gene expression of photosynthetic genes (Manzara et al., 1991), but to date no I-box binding protein has been cloned from plants."[2]
SRF is important during the development of the embryo, as it has been linked to the formation of mesoderm.[3][4]
The Serum response factor (SRF) has been shown to interact with GATA4.[5][6]
Cell specific developmental expression is tightly controlled, but, once expressed, require no additional activation -- GATA transcription factor (GATA), hepatocyte nuclear factors (HNF), PIT-1, MyoD, Myf5, Hox, winged-helix transcription factors.
The class of diverse Cys4 zinc fingers includes the family of GATA-factors.
In the diagram on the right, STAT5 may be involved with an erythropoiesis receptor, or Epo Receptor. Murine, members of the subfamily Murinae, Epo Receptor truncations and known functions are included. Erythroid differentiation depends on transcriptional regulator GATA1, zinc finger DNA binding domain binds specifically to DNA consensus sequence [AT]GATA[AG] promoter elements. In erythropoiesis, EpoR is best known for inducing survival of progenitors.
Some "putative wound-response elements including AGC box-like sequences28, TCA motif-like sequences28, carrot extensin gene wound-response elements (AT-rich motif, TTTTTTT, TGACGT)29, constitutive PAL footprint and elicitor-inducible PAL footprint31, and proteinase inhibitor II footprint31 have been found in cabch29 promoter. Some cis-elements related to organ and tissue-specific expression such as GATA motif-like sequence, ASF-1 binding site-like elements also existed in 5′ upstream region. Meanwhile, some basic transcriptional regulatory cis-elements including G box-like and GC box-like elements are located in this region."[7]
"A computer search for transcription promoter elements [...] showed the presence of a prominent TATA box 22 nucleotides upstream of the transcription start site and an Sp1 site at position -42 to -33. The 5'-flanking sequence also contains three E boxes with CANNTG consensus sequences at positions -464 to -459, -90 to -85, and -52 to -47 that have been marked as E box, E1 box, and E2 box, respectively [...]. In addition, the 5'-flanking region contains one or more GRE, XRE, GATA-1, GCN-4, PEA-3, AP1, and AP2 consensus motifs and also three imperfect CArG sites [...]."[8]
Single transcription factor transdifferentiation
Brief expression of a single transcription factor, the ELT-7 GATA factor, can convert the identity of fully differentiated, specialized non-endodermal cells of the pharynx into fully differentiated intestinal cells in intact larvae and adult roundworm Caenorhabditis elegans with no requirement for a dedifferentiated intermediate.[9]
"ELT-7, a GATA transcription factor that regulates terminal intestinal differentiation (Maduro and Rothman, 2002; Sommermann et al., 2010), activates an intestinal marker (elt-2::lacZ::GFP) in non-intestinal cells when briefly ectopically expressed via a heat-shock promoter at any embryonic, larval, or adult stage [...]."[9]
The "END-1 GATA transcription factor, which specifies the endoderm progenitor (Zhu et al., 1997), does not activate widespread intestinal gene expression after the MCT [...]."[9]
Cardiomyocytes
Cell-based in vivo therapies may provide a transformative approach to augment vascular and muscle growth and to prevent non-contractile scar formation by delivering transcription factors[10] or microRNAs[11] to the heart.[12] Cardiac fibroblasts, which represent 50% of the cells in the mammalian heart, can be reprogrammed into cardiomyocyte-like cells in vivo by local delivery of cardiac core transcription factors (GATA4, MEF2C, TBX5 and for improved reprogramming plus ESRRG, MESP1, Myocardin and ZFPM2) after coronary ligation.[10][13] These results implicated therapies that can directly remuscularize the heart without cell transplantation. However, the efficiency of such reprogramming turned out to be very low and the phenotype of received cardiomyocyte-like cells does not resemble those of a mature normal cardiomyocyte. Furthermore, transplantation of cardiac transcription factors into injured murine hearts resulted in poor cell survival and minimal expression of cardiac genes.[14]
Blood stem cells
Definitive hematopoiesis emerges during embryogenesis via an endothelial-to-hematopoietic transition. Combination of four transcription factors, GATA2, GFI1B, c-Fos, and ETV6, is sufficient to induce in vitro development leading to the formation of endothelial-like precursor cells, with the subsequent appearance of hematopoietic cells.[15] Transient expression of six transcription factors (RUNX1T1, HLF, LMO2, Prdm5, PBX1, ZFP36) and also N-Myc with MEIS1, to improve reprogramming efficacy, is sufficient to activate the gene networks governing hematopoietic stem cells functional identity in committed blood cells. This finding marks a significant step toward one of the most sought-after goals of regenerative medicine: the ability to produce hematopoietic stem cells suitable for transplantation, using more mature or differentiated blood cells to make up the shortfall of bone marrow transplants[16] It should be noted, however, that the transcription factors used in this study belong to a group of proto-oncogenes and therefore these cells could be dangerous to humans. Still to be answered are the precise contribution of each of the eight factors to the reprogramming process and whether approaches that do not rely on viruses and transcription factors can have similar success. It also is not yet known whether the same results can be achieved using human cells or whether other, non-blood cells can be reprogrammed to iHSCs.[17]
See also
References
- ↑ Robert G. K. Donald and Anthony R. Cashmore (1990). "Mutation of either G box or I box sequences profoundly affects expression from the Arabidopsis rbcS‐1A promoter". The EMBO Journal. 9 (6): 1717–1726. doi:10.1002/j.1460-2075.1990.tb08295.x. Retrieved 8 November 2018.
- ↑ Annkatrin Rose, Iris Meier and Udo Wienand (28 October 1999). "The tomato I-box binding factor LeMYBI is a member of a novel class of Myb-like proteins". The Plant Journal. 20 (6): 641–652. doi:10.1046/j.1365-313X.1999.00638.x. Retrieved 8 November 2018.
- ↑ Sepulveda JL, Vlahopoulos S, Iyer D, Belaguli N, Schwartz RJ (July 2002). "Combinatorial expression of GATA4, Nkx2-5, and serum response factor directs early cardiac gene activity". J. Biol. Chem. 277 (28): 25775–82. doi:10.1074/jbc.M203122200. PMID 11983708.
- ↑ Barron MR, Belaguli NS, Zhang SX, Trinh M, Iyer D, Merlo X, Lough JW, Parmacek MS, Bruneau BG, Schwartz RJ (March 2005). "Serum response factor, an enriched cardiac mesoderm obligatory factor, is a downstream gene target for Tbx genes". J. Biol. Chem. 280 (12): 11816–28. doi:10.1074/jbc.M412408200. PMID 15591049.
- ↑ Belaguli NS, Sepulveda JL, Nigam V, Charron F, Nemer M, Schwartz RJ (October 2000). "Cardiac tissue enriched factors serum response factor and GATA-4 are mutual coregulators". Mol. Cell. Biol. 20 (20): 7550–8. doi:10.1128/mcb.20.20.7550-7558.2000. PMC 86307. PMID 11003651.
- ↑ Morin S, Paradis P, Aries A, Nemer M (February 2001). "Serum response factor-GATA ternary complex required for nuclear signaling by a G-protein-coupled receptor". Mol. Cell. Biol. 21 (4): 1036–44. doi:10.1128/MCB.21.4.1036-1044.2001. PMC 99558. PMID 11158291.
- ↑ Guo Qing Tang, Yong Yan Bai & Shi Wei Loo (1 June 1996). "Functional properties of a cabbage chitinase promoter from cabbage (Brassica oleracea var. capitata)". Cell Research. 6 (9): 75–84. Retrieved 24 March 2019.
- ↑ Nibedita Lenka, Aruna Basu, Jayati Mullick, and Narayan G. Avadhani (22 November 1996). "The role of an E box binding basic helix loop helix protein in the cardiac muscle-specific expression of the rat cytochrome oxidase subunit VIII gene" (PDF). The Journal of Biological Chemistry. 271 (47): 30281–30289. doi:10.1074/jbc.271.47.30281. Retrieved 7 February 2019.
- ↑ 9.0 9.1 9.2 Misty R. Riddle, Abraham Weintraub, Ken C. Q. Nguyen, David H. Hall, and Joel H. Rothman (2013). "Transdifferentiation and remodeling of post-embryonic C. elegans cells by a single transcription factor". Development. 140 (24): 4844–9. doi:10.1242/dev.103010. Retrieved 29 December 2019.
- ↑ 10.0 10.1 Template:Cite doi
- ↑ Template:Cite doi
- ↑ Template:Cite doi
- ↑ Template:Cite doi
- ↑ Template:Cite doi
- ↑ Pereira, C. F., Chang, B., Qiu, J., Niu, X., Papatsenko, D., Hendry, C. E., ... & Moore, K. (2013). Induction of a hemogenic program in mouse fibroblasts. Cell stem cell, 13(2), 205-218. DOI: http://dx.doi.org/10.1016/j.stem.2013.05.024
- ↑ Jonah Riddell, Roi Gazit, Brian S. Garrison, et al., & Derrick J. Rossi (2014). Reprogramming Committed Murine Blood Cells to Induced Hematopoietic Stem Cells with Defined Factors. Cell, 157(30, 549–564, DOI: http://dx.doi.org/10.1016/j.cell.2014.04.006
- ↑ Boston Children's Hospital."Blood cells reprogrammed into blood stem cells in mice". ScienceDaily, 24 April 2014