User:Chem455cr/Euchromatin

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Distinction between Euchromatin and Heterochromatin

Euchromatin is a lightly packed form of chromatin (DNA, RNA, and protein) that is enriched in genes, and is often (but not always) under active transcription. Euchromatin stands in contrast to heterochromatin, which is tightly packed and less accessible for transcription. 92% of the human genome is euchromatic.[1]

In eukaryotes, euchromatin comprises the most active portion of the genome within the cell nucleus. In prokaryotes, euchromatin is the only form of chromatin present; this indicates that the heterochromatin structure evolved later along with the nucleus, possibly as a mechanism to handle increasing genome size.

Structure[edit]

Euchromatin is composed of repeating subunits known as nucleosomes, reminiscent of an unfolded set of beads on a string, that are approximately 11 nm in diameter.[2] At the core of these nucleosomes are a set of four histone protein pairs: H3, H4, H2A, and H2B.[2] Each core histone protein possesses a 'tail' structure, which can vary in several ways; it is thought that these variations act as "master control switches" through different methylation and acetylation states, which determine the overall arrangement of the chromatin.[2] Approximately 147 base pairs of DNA are wound around the histone octamers, or a little less than 2 turns of the helix.[3] Nucleosomes along the strand are linked together via the histone, H1,[4] and a short space of open linker DNA, ranging from around 0-80 base pairs. The key distinction between the structure of euchromatin and heterochromatin is that the nucleosomes in euchromatin are much more widely spaced, which allows for easier access of different protein complexes to the DNA strand and thus increased gene transcription.[2]

Appearance[edit]

Euchromatin resembles a set of beads on a string at large magnifications.[2] From farther away, it can resemble a ball of tangled thread, such as in some electron microscope visualizations.[5] In both optical and electron microscopic visualizations, euchromatin appears lighter in color than heterochromatin - which is also present in the nucleus and appears darkly[6] - due to its less compact structure[5]. When visualizing chromosomes, such as in a karyogram, cytogenetic banding is used to stain the chromosomes. Cytogenetic banding allows us to see which parts of the chromosome are made up of euchromatin or heterochromatin in order to differentiate chromosomal subsections, irregularities or rearrangements.[7] One such example is G banding, otherwise known as Giemsa staining where euchromatin appears lighter than heterochromatin.[8]

Appearance of Heterochromatin and Euchromatin Under Various Visualization Techniques[8][9][10][11][12][13]
Giemsa (G-) Banding Reverse (R-) Banding Constitutive Heterochromatin (C-) banding Quinacrine (Q-) banding Telomeric R (T-) banding
Euchromatin Lighter Darker Lighter Dull Light
Heterochromatin Darker Lighter Darker Bright (Fluorescent) Darker (Faint)

Function[edit]

Transcription[edit]

Euchromatin participates in the active transcription of DNA to mRNA products. The unfolded structure allows gene regulatory proteins and RNA polymerase complexes to bind to the DNA sequence, which can then initiate the transcription process.[2] While not all euchromatin is necessarily transcribed, as the euchromatin is divided into transcriptionally active and inactive domains,[14] euchromatin is still generally associated with active gene transcription. There is therefore a direct link to how actively productive a cell is and the amount of euchromatin that can be found in its nucleus.

It is thought that the cell uses transformation from euchromatin into heterochromatin as a method of controlling gene expression and replication, since such processes behave differently on densely compacted chromatin. This is known as the 'accessibility hypothesis'.[15] One example of constitutive euchromatin that is 'always turned on' is housekeeping genes, which code for the proteins needed for basic functions of cell survival.[16]

Epigenetics[edit]

Epigenetics involves changes in the phenotype that can be inherited without changing the DNA sequence. This can occur through many types of environmental interactions.[17] Regarding euchromatin, post-translational modifications of the histones can alter the structure of chromatin, resulting in altered gene expression without changing the DNA.[18] Additionally, a loss of heterochromatin and increase in euchromatin has been shown to correlate with an accelerated aging process, especially in diseases known to resemble premature aging.[19] Research has shown epigenetic markers on histones for a number of additional diseases.[20][21]

Regulation[edit]

Euchromatin is primarily regulated by post-translational modifications to its nucleosomes’ histones, conducted by many histone-modifying enzymes. These modifications occur on the histones’ N-terminal tails that protrude from the nucleosome structure, and are thought of to recruit enzymes to either keep the chromatin in its open form, as euchromatin, or in its closed form, as heterochromatin.[22] Histone acetylation, for instance, is typically associated with euchromatin structure, whereas histone methylation promotes heterochromatin remodeling.[23] Acetylation makes the histone group more negatively charged, which in turn disrupts its interactions with the DNA strand, essentially “opening” the strand for easier access.[22] Acetylation can occur on multiple lysine residues of a histone’s N-terminal tail and in different histones of the same nucleosome, which is thought to further increase DNA accessibility for transcription factors.[22]

Phosphorylation of histones is another method by which euchromatin is regulated.[22] This tends to occur on the N-terminal tails of the histones, however some sites are present in the core.[22] Phosphorylation is controlled by kinases and phosphatases, which add and remove the phosphate groups respectively. This can occur at serine, threonine, or tyrosine residues present in euchromatin.[22][23] Since the phosphate groups added to the structure will incorporate a negative charge, it will promote the more relaxed “open” form, similar to acetylation.[23] In regards to functionality, histone phosphorylation is involved with gene expression, DNA damage repair, and chromatin remodeling.[23]

Another method of regulation that incorporates a negative charge, thereby favoring the “open” form, is ADP ribosylation.[23] This process adds one or more ADP-ribose units to the histone, and is involved in the DNA damage response pathway.[23]

Additional Links and Information[edit]

  • Histone Modifying Enzymes
  • Constitutive Heterochromatin
  • Heterochromatin formation involves changes in histone modifications over multiple cell generations[24]
  • Chromatin Velocity reveals epigenetic dynamics by single-cell profiling of heterochromatin and euchromatin[25]
  • Epigenetic inheritance and the missing heritability[26]
  • Histone epigenetic marks in heterochromatin and euchromatin of the Chagas' disease vector, Triatoma infestans[27]

References[edit]

  1. ^ International Human Genome Sequencing Consortium (2004). "Finishing the euchromatic sequence of the human genome". Nature. 431: 931–945. doi:10.1038/nature03001. ISSN 0028-0836.
  2. ^ a b c d e f Babu, Arvind; Verma, Ram S. (1987-01-01), Bourne, G. H.; Jeon, K. W.; Friedlander, M. (eds.), "Chromosome Structure: Euchromatin and Heterochromatin", International Review of Cytology, vol. 108, Academic Press, pp. 1–60, retrieved 2021-10-06
  3. ^ "nucleosome / nucleosomes | Learn Science at Scitable". www.nature.com. Retrieved 2021-10-06.
  4. ^ Mobley, Arie S. (2019-01-01), Mobley, Arie S. (ed.), "Chapter 4 - Induced Pluripotent Stem Cells", Neural Stem Cells and Adult Neurogenesis, Academic Press, pp. 67–94, ISBN 978-0-12-811014-0, retrieved 2021-10-06
  5. ^ a b "The cell. 4. Nucleus. Chromatin. Atlas of plant and animal histology". mmegias.webs.uvigo.es. Retrieved 2021-12-02.
  6. ^ Enukashvily, Natella I.; Ponomartsev, Nikita V. (2013-01-01), Donev, Rossen (ed.), "Chapter Two - Mammalian Satellite DNA: A Speaking Dumb", Advances in Protein Chemistry and Structural Biology, Organisation of Chromosomes, vol. 90, Academic Press, pp. 31–65, retrieved 2021-10-06
  7. ^ Shen, Chang-Hui (2019-01-01), Shen, Chang-Hui (ed.), "Chapter 13 - Molecular Diagnosis of Chromosomal Disorders", Diagnostic Molecular Biology, Academic Press, pp. 331–358, ISBN 978-0-12-802823-0, retrieved 2021-10-06
  8. ^ a b "Giemsa banding". Biology Articles, Tutorials & Dictionary Online. 2019-10-07. Retrieved 2021-12-02.
  9. ^ "Reverse banding - Definition and Examples - Biology Online Dictionary". Biology Articles, Tutorials & Dictionary Online. 2020-09-18. Retrieved 2021-12-02.
  10. ^ "Constitutive heterochromatin banding". Biology Articles, Tutorials & Dictionary Online. 2019-10-07. Retrieved 2021-12-02.
  11. ^ "Quinacrine banding". Biology Articles, Tutorials & Dictionary Online. 2019-10-07. Retrieved 2021-12-02.
  12. ^ "T-banding". Biology Articles, Tutorials & Dictionary Online. 2019-10-07. Retrieved 2021-12-02.
  13. ^ Babu, Arvind; Verma, Ram S. (1987-01-01), Bourne, G. H.; Jeon, K. W.; Friedlander, M. (eds.), "Chromosome Structure: Euchromatin and Heterochromatin", International Review of Cytology, vol. 108, Academic Press, pp. 1–60, retrieved 2021-12-02
  14. ^ Verschure, Pernette J.; van der Kraan, Ineke; Manders, Erik M.M.; van Driel, Roel (1999-10-04). "Spatial Relationship between Transcription Sites and Chromosome Territories". Journal of Cell Biology. 147 (1): 13–24. doi:10.1083/jcb.147.1.13. ISSN 0021-9525. PMC 2164981. PMID 10508851.{{cite journal}}: CS1 maint: PMC format (link)
  15. ^ Muegge, Kathrin (2003-04-01). "Modifications of histone cores and tails in V(D)J recombination". Genome Biology. 4 (4): 211. doi:10.1186/gb-2003-4-4-211. ISSN 1474-760X. PMC 154571. PMID 12702201.{{cite journal}}: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link)
  16. ^ Eisenberg, Eli; Levanon, Erez Y. (2013-10-01). "Human housekeeping genes, revisited". Trends in Genetics. 29 (10): 569–574. doi:10.1016/j.tig.2013.05.010. ISSN 0168-9525. PMID 23810203.
  17. ^ Arney, Katharine L.; Fisher, Amanda G. (2004-09-01). "Epigenetic aspects of differentiation". Journal of Cell Science. 117 (19): 4355–4363. doi:10.1242/jcs.01390. ISSN 0021-9533.
  18. ^ Singh, Narendra Pratap; Madabhushi, Sri Ranganayaki; Srivastava, Surabhi; Senthilkumar, R.; Neeraja, C.; Khosla, Sanjeev; Mishra, Rakesh K. (2011). "Epigenetic profile of the euchromatic region of human Y chromosome". Nucleic Acids Research. 39 (9): 3594–3606. doi:10.1093/nar/gkq1342. ISSN 0305-1048. PMC 3089472. PMID 21252296.
  19. ^ Wang, Jiyong; Jia, Sharon T.; Jia, Songtao (2016-05-01). "New Insights into the Regulation of Heterochromatin". Trends in Genetics. 32 (5): 284–294. doi:10.1016/j.tig.2016.02.005. ISSN 0168-9525.
  20. ^ "Epigenetic Influences and Disease | Learn Science at Scitable". www.nature.com. Retrieved 2021-12-02.
  21. ^ Alaskhar Alhamwe, Bilal; Khalaila, Razi; Wolf, Johanna; von Bülow, Verena; Harb, Hani; Alhamdan, Fahd; Hii, Charles S.; Prescott, Susan L.; Ferrante, Antonio; Renz, Harald; Garn, Holger (2018-05-23). "Histone modifications and their role in epigenetics of atopy and allergic diseases". Allergy, Asthma & Clinical Immunology. 14 (1): 39. doi:10.1186/s13223-018-0259-4. ISSN 1710-1492. PMC 5966915. PMID 29796022.{{cite journal}}: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link)
  22. ^ a b c d e f Bannister, Andrew J.; Kouzarides, Tony (2011). "Regulation of chromatin by histone modifications". Cell Research. 21 (3): 381–395. doi:10.1038/cr.2011.22. ISSN 1748-7838.
  23. ^ a b c d e f Singh, Dipty; Nishi, Kumari; Khambata, Kushaan; Balasinor, N. H. (2020-01-01), Tollefsbol, Trygve (ed.), "Introduction to epigenetics: basic concepts and advancements in the field", Epigenetics and Reproductive Health, Translational Epigenetics, vol. 21, Academic Press, pp. xxv–xliv, retrieved 2021-10-06
  24. ^ Katan-Khaykovich, Yael; Struhl, Kevin (2005-06-15). "Heterochromatin formation involves changes in histone modifications over multiple cell generations". The EMBO Journal. 24 (12): 2138–2149. doi:10.1038/sj.emboj.7600692. ISSN 0261-4189. PMC 1150886. PMID 15920479.
  25. ^ Tedesco, Martina; Giannese, Francesca; Lazarević, Dejan; Giansanti, Valentina; Rosano, Dalia; Monzani, Silvia; Catalano, Irene; Grassi, Elena; Zanella, Eugenia R.; Botrugno, Oronza A.; Morelli, Leonardo (2021-10-11). "Chromatin Velocity reveals epigenetic dynamics by single-cell profiling of heterochromatin and euchromatin". Nature Biotechnology: 1–10. doi:10.1038/s41587-021-01031-1. ISSN 1546-1696.
  26. ^ Trerotola, Marco; Relli, Valeria; Simeone, Pasquale; Alberti, Saverio (2015-07-28). "Epigenetic inheritance and the missing heritability". Human Genomics. 9 (1): 17. doi:10.1186/s40246-015-0041-3. ISSN 1473-9542. PMC 4517414. PMID 26216216.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  27. ^ Alvarenga, Elenice M.; Rodrigues, Vera L. C. C.; Moraes, Alberto S.; Naves, Luisa S.; Mondin, Mateus; Felisbino, Marina B.; Mello, Maria Luiza S. (2016-04-11). "Histone epigenetic marks in heterochromatin and euchromatin of the Chagas' disease vector, Triatoma infestans". Acta Histochemica. 118 (4): 401–412. doi:10.1016/j.acthis.2016.04.002. ISSN 1618-0372. PMID 27079857.
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