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Pioneer transcription factors open up a region of compacted chromatin to allow other transcription factors to bind to the exposed DNA

Pioneer transcription factors are proteins that function in the nucleus of eukaryotic cells to regulate gene expression at the level of transcription. Pioneers are different than other transcription factors and general transcription factors in that the pioneers can bind to "closed" (or "compacted" or "condensed") euchromatin.[1][a] The first two[b] were named "pioneer" factors in 2002 because they were found to be capable of binding to target sites on compacted nucleosomal DNA in vitro and opening the chromatin needed for some transcription during liver development.[2] Some, but not all, pioneer factors act in a unidirectional manner from their binding site.[1] Pioneer factors are involved in initiating cell differentiation, cell reprogramming and induction of pluripotent stem cells.[1]

The eukaryotic cell condenses its genome by wrapping it around nucleosomes into a "10 nm fiber" and then into more tightly packed chromatin. The canonical tightly packed chromatin has been described as a "30 nm fiber", but the existence of that structure is under debate.[3][4][5][6][c] In any case, the structure of chromatin changes during the cell cycle, and one function of pioneers is to "bookmark" sites on chromosomes that are to become active when the cells enter the appropriate phase of the cell cycle.[1]

FoxA protein - formerly Active rearrangement

I am working on this former "Active rearrangement" section starting 3/9/17. Dennis

An animation of a DNA strand unwrapping from a histone complex.

FoxA, one of the first named pioneers, is a member of the family of FOX proteins that contain the DNA-binding fork head domain.[d] That domain is similar to part of the "linker" histone H1, and the ability of FoxA to displace H1 is crucial for its pioneering function.[1][e] This displacement is an ATP-independent process.[1] Fork head domains have a segment that confers DNA sequence specificity for binding, unlike linker histone,[7][8], which may explain the lack of ATP energy requirement.

There are several reports that show initial binding of FoxA preceeds binding of other gene-regulatory proteins to their targets.reviewed in[1] More recently, it was shown that FoxA binding is required for binding of liver-specific tanscription factors.[9] These and other studies lead to the concepts that FoxA and other factors bind coordinately and cooperatively to their target sites.[1][f]

As might be anticipated by its importance for binding of liver-specific transciption factors, FoxA is involved in 2 biologic processes related to liver development or hepatocytes.[1]. In mouse fibroblasts, FoxA induces transdifferentiation of the fibroblasts into hepatocyte-like cells.[1] During mouse development, FoxA is important for development of the liver.[1]

FoxA is one of the known bookmarking factors.[1] Most of the FoxA that is bound to DNA during interphase becomes dissociated during mitosis[10] However, what remains bound is important for reactivation of expression of the FoxA target genes quickly after mitosis[10][g]


The following is a repeat of the PF article, including the March 5, 2017 00:27 edit (+1,564)‎ by Boghog‎ (consistent citation formatting), to be used during upgrading, March 2017

Note of 3/12/17: I will make comments in the body of the former article below, which I will indicate by using (DP comment: small italic text).

Opening of condensed chromatin by a pioneer factor to initiate transcription. The pioneer factor binds to tightly packed chromatin and causes a nucleosomal rearrangement. This new configuration allows space for other transcription factors to bind and initiate transcription.

Pioneer factors are transcription factors that can directly bind condensed chromatin. They can have positive and negative effects on transcription and are important in recruiting other transcription factors and histone modification enzymes as well as controlling DNA methylation. They were first discovered in 2002 as factors capable of binding to target sites on nucleosomal DNA in compacted chromatin and endowing competency for gene activity during hepatogenesis.[12] Pioneer factors are involved in initiating cell differentiation and activation of cell-specific genes. This property is observed in fork head box (FOX), Groucho TEL, and in Gal4 transcription factors.[13]

The eukaryotic cell condenses its genome into tightly packed chromatin and nucleosomes. This ability saves space in the nucleus for only actively transcribed genes and hides unnecessary or detrimental genes from being transcribed. Access to these condensed regions is done by chromatin remodelling by either balancing histone modifications or directly with pioneer factors that can loosen the chromatin themselves or as a flag recruiting other factors. Pioneer factors are not necessarily required for assembly of the transcription apparatus and may dissociate after being replaced by other factors.

Passive factors

An example of the cell ‘priming’ for rapidly induced transcription. The pioneer factor, FoxA1 binds the enhancer in the first step but can not initiate transcription. Next when the signal, estrogen, is present the estrogen receptor can quickly find the ‘bookmark’ pioneer factor. When the estrogen receptor is bound transcription is initiated.

Pioneer factors can function in a passively acting as a bookmark for the cell to recruit other transcription factors to specific genes in condensed chromatin. This can be important for priming the cell for a rapid response as the enhancer is already bound by a pioneer transcription factor giving it a head start towards assembling the transcription preinitiation complex. Hormone responses are often quickly induced in the cell using this priming method such as with the estrogen receptor.[14](DP comment: This appears to be true so far, but since I've made FoxA the focus of introducing this bookmarking/priming function, I will not include this discussion) Another form of priming is when an enhancer is simultaneously bound by activating and repressing pioneer factors. This balance can be tipped by dissociation of one of the factors. In hepatic cell differentiation the activating pioneer factor FOXA1 recruites a repressor, grg3, that prevents transcription until the repressor is down-regulated later on in the differentiation process.[15](DP comment: The reference cited for grg3 is from the Zaret lab, but says nothing about grg3, and the 2014 review by Zaret does not cite this reference. Thus, I will not include this discussion)
In a direct role pioneer factors can bind an enhancer and recruit activation complex that will modify the chromatin directly. The change in the chromatin changes the affinity, decreasing the affinity of the pioneer factor such that it is replaced by a transcription factor that has a higher affinity. This is a mechanism for the cell to switch a gene on was observed with glucocorticoid receptor recruiting modification factors that then modify the site to bind activated estrogen receptor which was coined as a “bait and switch” mechanism.[16](DP comment: The reference cited for "bait and switch" does not use the words "bait" or "switch". The reference is about the glucocorticoid receptor, but I can find no evidence of it being a pioneer. sigh. Obviously, I won't use this. It pisses me off that so many people have read this crud. This finishes off the entire Passive factors section)

Epigenetic effects

Pioneer factor, PU.1, binding cell-specific gene regulation in hematopoietic differentiation. In hematopoietic stem cells PU.1 binds different lineage-specific enhancers and recruits histone modification enzymes that mark these enhancers with H3K4me1. These modified histones are then recognized by cell-specific transcription factors that activate genes leading to the differentiation of B-cells or macrophages.

Pioneer factors can exhibit their greatest range of effects on transcription through the modulation of epigenetic factors by recruiting activating or repressing histone modification enzymes and controlling CpG methylation by protecting specific cysteine residues. This has effects on controlling the timing of transcription during cell differentiation processes.

Histone modification

Histone modification is a well-studied mechanism to transiently adjust chromatin density. Pioneer factors can play a role in this by binding specific enhancers and flagging histone modification enzymes to that specific gene. Repressive pioneer factors can inhibit transcription by recruiting factors that modify histones that further tighten the chromatin. This is important to limit gene expression to specific cell types and has to be removed only when cell differentiation begins. FoxD3 has been associated as a repressor of both B-cell and melanocytic cell differentiation pathways, maintaining repressive histone modifications where bound, that have to be overcome to start differentiation.[17][18](DP comment: FoxD3 is a transcription factor, but I cannot find anybody other than the editor who wrote the preceeding passage calling it a pioneer, so I won't be including it.) Pioneer factors can also be associated with recruiting transcription-activating histone modifications. Enzymes that modify H3K4 with mono and di-methylation are associated with increasing transcription and have been shown to bind pioneer factors.[14](DP comment: "Enzymes ...yada yada... have been shown to bind pioneer factors" is not found in the referenced paper and as far as I can see is untrue. siiggghhhh.....) In B cell differentiation PU.1 is necessary to signal specific histones for activating H3K4me1 modifications that differentiate hematopoietic stem cells into either the B-cell or macrophage lineage.[19] FoxA1 binding induces HSK4me2 during neuronal differentiation of pluripotent stem cells [20] as well as the loss of DNA methylation.[21]

DNA methylation

Pioneer factors can also affect transcription and differentiation through the control of DNA methylation. Pioneer factors that bind to CpG islands and cysteine residues block access to methyltransferases. Many eukaryotic cells have CpG islands in their promoters that can be modified by methylation having adverse effects on their ability to control transcription.[22] This phenomenon is also present in promoters without CpG islands where single cysteine residues are protected from methylation until further cell differentiation. An example is FoxD3 preventing methylation of a cysteine residue in Alb1 enhancer, acting as a place holder for FoxA1 later in hepatic [23] as well as in CpG islands of genes in chronic lymphocytic leukemia.[24] For stable control of methylation state the cysteine residues are covered during mitosis, unlike most other transcription factors, to prevent methylation. Studies have shown that during mitosis 15% of all interphase FoxA1 binding sites were bound.[25] The protection of cysteine methylation can be quickly removed allowing for rapid induction when a signal is present.

Other pioneer factors

A well studied pioneer factor family is the Goucho-related (Gro/TLE/Grg) transcription factors that often have a negative effect on transcription. These chromatin binding domains can span up to 3-4 nucleosomes. These large domains are scaffolds for further protein interactions and also modify the chromatin for other pioneer factors such as FoxA1 which has been shown to bind to Grg3.[26] Transcription factors with zinc finger DNA binding domains, such as the GATA family and glucocorticoid receptor.[14] The zinc finger domains do not appear to bind nucleosomes well and can be displaced by FOX factors.[25]

Role in cancer

The ability of pioneer factors to respond to extracellular signals to differentiate cell type has been studied as a potential component of hormone-dependent cancers. Hormones such as estrogen and IGFI are shown to increase pioneer factor concentration leading to a change in transcription.[27] Known pioneer factors such as FoxA1, PBX1, TLE, AP2ɣ, GATA factors 2/3/4, and PU.1 have been associated with hormone-dependent cancer . FoxA1 is necessary for estrogen and androgen mediated hepatocarcinogenesis and is a defining gene for ER+ luminal breast cancer, as is another pioneer factor GATA3.[14][27] FOXA1 particularly is expressed in 90% of breast cancer metastases and 89% of metastic prostate cancers.[27][28] In the breast cancer cell line, MCF-7, it was found that FoxA1 was bound to 50% of estrogen receptor binding sites independent of estrogen presence. High expression of pioneer factors is associated with poor prognosis with the exception of breast cancer where FoxA1 is associated with a stronger outcome.[27]
The correlation between pioneer factors and cancer has led to prospective therapeutic targeting. In knockdown studies in the MCF-7 breast cancer cell line it was found that decreasing pioneer factors FoxA1 and AP2ɣ decreased ER signalling.[13][27] Other fork head proteins have been associated with cancer, including FoxO3 and FoxM that repress the cell survival pathways Ras and PPI3K/AKT/IKK.[29] Drugs such as Paclitaxel, Imatinib, and doxorubicin which activate FoxO3a or its targets are being used. Modification to modulate related factors with pioneer activity is a topic of interest in the early stages as knocking down pioneer factors may have toxic effects through alteration of the lineage pathways of healthy cells.[27]


Notes

  1. ^ closed euchromatin is different than heterochromatin
  2. ^ The first 2 pioneers investigated were HNF3 (FoxA) and GATA4. HNF3 was the more intensely studied of the 2 and has become more commonly known as FoxA, which is the name that will be used in this article.
  3. ^ The uncertainty of chromatin structure is reflected in the atypical and irregular depiction of compacted chromatin in the figure.
  4. ^ "FOX" comes from FOrkhead boX.
  5. ^ This displacement is the first step that will be shown in slashme's new video, at which time this efn will be modified to "This displacement is the first step shown in the video"
  6. ^ The video illustrates how initial binding of FoxA to a nucleosome initiates changes in the structure that can allow another factor to bind while the nucleosome is still mostly intact.
  7. ^ Similar bookmarking functions for one of the GATA family of pioneer transcription factors have been reported[11]

References

  1. ^ a b c d e f g h i j k l Iwafuchi-Doi M, Zaret KS (2014). "Pioneer transcription factors in cell reprogramming". Genes Dev. pp. 2679–92. doi:10.1101/gad.253443.114. PMID 25512556.
  2. ^ Cirillo LA, Lin FR, Cuesta I, Friedman D, Jarnik M, Zaret KS (February 2002). "Opening of Compacted Chromatin by Early Developmental Transcription Factors HNF3 (FoxA) and GATA-4" (PDF). Molecular Cell. pp. 279–89. doi:10.1016/S1097-2765(02)00459-8. PMID 11864602.{{cite web}}: CS1 maint: multiple names: authors list (link)
  3. ^ Luger K, Dechassa ML, Tremethick DJ. (2012). "New insights into nucleosome and chromatin structure: an ordered state or a disordered affair?". Nat Rev Mol Cell Biol. 13 (7): 436–47. doi:10.1038/nrm3382. PMID 22722606.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^ Nishino Y, Eltsov M, Joti Y, Ito K, Takata H, Takahashi Y, Hihara S, Frangakis AS, Imamoto N, Ishikawa T, Maeshima K. (2012). "Human mitotic chromosomes consist predominantly of irregularly folded nucleosome fibres without a 30-nm chromatin structure". EMBO J. 31 (7): 1644–53. doi:10.1038/emboj.2012.35. PMID 22343941.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. ^ Li G, Zhu P (2015). "Structure and organization of chromatin fiber in the nucleus". FEBS lett. 589: 2893–904. doi:10.1016/j.febslet.2015.04.023. PMID 25913782.
  6. ^ Risca VI, Denny SK, Straight AF, Greenleaf WJ (2017). "Variable chromatin structure revealed by in situ spatially correlated DNA cleavage mapping". Nature. 541 (7636): 237–241. doi:10.1038/nature20781. PMID 28024297.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  7. ^ Cite error: The named reference Clark was invoked but never defined (see the help page).
  8. ^ Sekiya T, Muthurajan UM, Luger K, Tulin AV, Zaret KS (April 2009). "Nucleosome-binding affinity as a primary determinant of the nuclear mobility of the pioneer transcription factor FoxA". Genes & Development. 23 (7): 804–9. doi:10.1101/gad.1775509. PMC 2666343. PMID 19339686.
  9. ^ Iwafuchi-Doi M, Donahue G, Kakumanu A, Watts JA, Mahony S, Pugh BF, Lee D, Kaestner KH, Zaret KS (2016). "The Pioneer Transcription Factor FoxA Maintains an Accessible Nucleosome Configuration at Enhancers for Tissue-Specific Gene Activation". Mol Cell. 62 (1): 79–91. doi:10.1016/j.molcel.2016.03.001. PMID 27058788.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  10. ^ a b Caravaca JM, Donahue G, Becker JS, He X, Vinson C, Zaret KS. (2013). "Bookmarking by specific and nonspecific binding of FoxA1 pioneer factor to mitotic chromosomes". Genes Dev. pp. 251–60. doi:10.1101/gad.206458.112.{{cite web}}: CS1 maint: multiple names: authors list (link)
  11. ^ Kadauke S, Udugama MI, Pawlicki JM, Achtman JC, Jain DP, Cheng Y, Hardison RC, Blobel GA. (2012). "Tissue-specific mitotic bookmarking by hematopoietic transcription factor GATA1". Cell. 150 (4): 725–37. doi:10.1016/j.cell.2012.06.038. PMID 22901805.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  12. ^ Cirillo LA, Lin FR, Cuesta I, Friedman D, Jarnik M, Zaret KS (February 2002). "Opening of compacted chromatin by early developmental transcription factors HNF3 (FoxA) and GATA-4". Molecular Cell. 9 (2): 279–89. doi:10.1016/S1097-2765(02)00459-8. PMID 11864602.
  13. ^ a b Magnani L, Eeckhoute J, Lupien M (November 2011). "Pioneer factors: directing transcriptional regulators within the chromatin environment". Trends in Genetics. 27 (11): 465–74. doi:10.1016/j.tig.2011.07.002. PMID 21885149.
  14. ^ a b c d Zaret KS, Carroll JS (November 2011). "Pioneer transcription factors: establishing competence for gene expression". Genes & Development. 25 (21): 2227–41. doi:10.1101/gad.176826.111. PMC 3219227. PMID 22056668.
  15. ^ Xu CR, Cole PA, Meyers DJ, Kormish J, Dent S, Zaret KS (May 2011). "Chromatin "prepattern" and histone modifiers in a fate choice for liver and pancreas". Science. 332 (6032): 963–6. doi:10.1126/science.1202845. PMC 3128430. PMID 21596989.
  16. ^ Voss TC, Schiltz RL, Sung MH, Yen PM, Stamatoyannopoulos JA, Biddie SC, Johnson TA, Miranda TB, John S, Hager GL (August 2011). "Dynamic exchange at regulatory elements during chromatin remodeling underlies assisted loading mechanism". Cell. 146 (4): 544–54. doi:10.1016/j.cell.2011.07.006. PMC 3210475. PMID 21835447.
  17. ^ Liber D, Domaschenz R, Holmqvist PH, Mazzarella L, Georgiou A, Leleu M, Fisher AG, Labosky PA, Dillon N (July 2010). "Epigenetic priming of a pre-B cell-specific enhancer through binding of Sox2 and Foxd3 at the ESC stage". Cell Stem Cell. 7 (1): 114–26. doi:10.1016/j.stem.2010.05.020. PMID 20621055.
  18. ^ Katiyar P, Aplin AE (May 2011). "FOXD3 regulates migration properties and Rnd3 expression in melanoma cells". Molecular Cancer Research. 9 (5): 545–52. doi:10.1158/1541-7786.MCR-10-0454. PMC 3096755. PMID 21478267.
  19. ^ Heinz S, Benner C, Spann N, Bertolino E, Lin YC, Laslo P, Cheng JX, Murre C, Singh H, Glass CK (May 2010). "Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identities". Molecular Cell. 38 (4): 576–89. doi:10.1016/j.molcel.2010.05.004. PMC 2898526. PMID 20513432.
  20. ^ Sérandour AA, Avner S, Percevault F, Demay F, Bizot M, Lucchetti-Miganeh C, Barloy-Hubler F, Brown M, Lupien M, Métivier R, Salbert G, Eeckhoute J (April 2011). "Epigenetic switch involved in activation of pioneer factor FOXA1-dependent enhancers". Genome Research. 21 (4): 555–65. doi:10.1101/gr.111534.110. PMC 3065703. PMID 21233399.
  21. ^ Taube JH, Allton K, Duncan SA, Shen L, Barton MC (May 2010). "Foxa1 functions as a pioneer transcription factor at transposable elements to activate Afp during differentiation of embryonic stem cells". The Journal of Biological Chemistry. 285 (21): 16135–44. doi:10.1074/jbc.M109.088096. PMC 2871482. PMID 20348100.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  22. ^ Smale ST (October 2010). "Pioneer factors in embryonic stem cells and differentiation". Current Opinion in Genetics & Development. 20 (5): 519–26. doi:10.1016/j.gde.2010.06.010. PMC 2943026. PMID 20638836.
  23. ^ Xu J, Watts JA, Pope SD, Gadue P, Kamps M, Plath K, Zaret KS, Smale ST (December 2009). "Transcriptional competence and the active marking of tissue-specific enhancers by defined transcription factors in embryonic and induced pluripotent stem cells". Genes & Development. 23 (24): 2824–38. doi:10.1101/gad.1861209. PMC 2800090. PMID 20008934.
  24. ^ Chen SS, Raval A, Johnson AJ, Hertlein E, Liu TH, Jin VX, Sherman MH, Liu SJ, Dawson DW, Williams KE, Lanasa M, Liyanarachchi S, Lin TS, Marcucci G, Pekarsky Y, Davuluri R, Croce CM, Guttridge DC, Teitell MA, Byrd JC, Plass C (August 2009). "Epigenetic changes during disease progression in a murine model of human chronic lymphocytic leukemia". Proceedings of the National Academy of Sciences of the United States of America. 106 (32): 13433–8. doi:10.1073/pnas.0906455106. PMC 2726368. PMID 19666576.
  25. ^ a b Caravaca JM, Donahue G, Becker JS, He X, Vinson C, Zaret KS (February 2013). "Bookmarking by specific and nonspecific binding of FoxA1 pioneer factor to mitotic chromosomes". Genes & Development. 27 (3): 251–60. doi:10.1101/gad.206458.112. PMID 23355396.
  26. ^ Sekiya T, Zaret KS (October 2007). "Repression by Groucho/TLE/Grg proteins: genomic site recruitment generates compacted chromatin in vitro and impairs activator binding in vivo". Molecular Cell. 28 (2): 291–303. doi:10.1016/j.molcel.2007.10.002. PMC 2083644. PMID 17964267.
  27. ^ a b c d e f Jozwik KM, Carroll JS (May 2012). "Pioneer factors in hormone-dependent cancers". Nature Reviews. Cancer. 12 (6): 381–5. doi:10.1038/nrc3263. PMID 22555282.
  28. ^ Ross-Innes CS, Stark R, Teschendorff AE, Holmes KA, Ali HR, Dunning MJ, Brown GD, Gojis O, Ellis IO, Green AR, Ali S, Chin SF, Palmieri C, Caldas C, Carroll JS (January 2012). "Differential oestrogen receptor binding is associated with clinical outcome in breast cancer". Nature. 481 (7381): 389–93. doi:10.1038/nature10730. PMC 3272464. PMID 22217937.
  29. ^ Yang JY, Hung MC (February 2009). "A new fork for clinical application: targeting forkhead transcription factors in cancer". Clinical Cancer Research. 15 (3): 752–7. doi:10.1158/1078-0432.CCR-08-0124. PMC 2676228. PMID 19188143.
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