Heterochromatin

August 20, 2022
by

Heterochromatin is a tightly packed form of DNA or condensed DNA, which comes in multiple varieties. These varieties lie on a continuum between the two extremes of constitutive heterochromatin and facultative heterochromatin. Both play a role in the expression of genes. Because it is tightly packed, it was thought to be inaccessible to polymerases and therefore not transcribed; however, according to Volpe et al. (2002),[1] and many other papers since,[2] much of this DNA is in fact transcribed, but it is continuously turned over via RNA-induced transcriptional silencing (RITS). Recent studies with electron microscopy and OsO4 staining reveal that the dense packing is not due to the chromatin.[3]

Constitutive heterochromatin can affect the genes near itself (e.g. position-effect variegation). It is usually repetitive and forms structural functions such as centromeres or telomeres, in addition to acting as an attractor for other gene-expression or repression signals.

Facultative heterochromatin is the result of genes that are silenced through a mechanism such as histone deacetylation or Piwi-interacting RNA (piRNA) through RNAi. It is not repetitive and shares the compact structure of constitutive heterochromatin. However, under specific developmental or environmental signaling cues, it can lose its condensed structure and become transcriptionally active.[4]


Heterochromatin has been associated with the di- and tri -methylation of H3K9 in certain portions of the human genome.[5] H3K9me3-related methyltransferases appear to have a pivotal role in modifying heterochromatin during lineage commitment at the onset of organogenesis and in maintaining lineage fidelity.[6]

Structure

Chromatin is found in two varieties: euchromatin and heterochromatin.[7] Originally, the two forms were distinguished cytologically by how intensely they get stained – the euchromatin is less intense, while heterochromatin stains intensely, indicating tighter packing. Heterochromatin is usually localized to the periphery of the nucleus. Despite this early dichotomy, recent evidence in both animals[8] and plants[9] has suggested that there are more than two distinct heterochromatin states, and it may in fact exist in four or five ‘states’, each marked by different combinations of epigenetic marks.

Heterochromatin mainly consists of genetically inactive satellite sequences,[10] and many genes are repressed to various extents, although some cannot be expressed in euchromatin at all.[11] Both centromeres and telomeres are heterochromatic, as is the Barr body of the second, inactivated X-chromosome in a female.

Function

Heterochromatin has been associated with several functions, from gene regulation to the protection of chromosome integrity;[12] some of these roles can be attributed to the dense packing of DNA, which makes it less accessible to protein factors that usually bind DNA or its associated factors. For example, naked double-stranded DNA ends would usually be interpreted by the cell as damaged or viral DNA, triggering cell cycle arrest, DNA repair or destruction of the fragment, such as by endonucleases in bacteria.

Some regions of chromatin are very densely packed with fibers that display a condition comparable to that of the chromosome at mitosis. Heterochromatin is generally clonally inherited; when a cell divides, the two daughter cells typically contain heterochromatin within the same regions of DNA, resulting in epigenetic inheritance. Variations cause heterochromatin to encroach on adjacent genes or recede from genes at the extremes of domains. Transcribable material may be repressed by being positioned (in cis) at these boundary domains. This gives rise to expression levels that vary from cell to cell,[13] which may be demonstrated by position-effect variegation.[14] Insulator sequences may act as a barrier in rare cases where constitutive heterochromatin and highly active genes are juxtaposed (e.g. the 5’HS4 insulator upstream of the chicken β-globin locus,[15] and loci in two Saccharomyces spp.[16][17]).

Constitutive heterochromatin

Main article: Constitutive heterochromatin

All cells of a given species package the same regions of DNA in constitutive heterochromatin, and thus in all cells, any genes contained within the constitutive heterochromatin will be poorly expressed. For example, all human chromosomes 1, 9, 16, and the Y-chromosome contain large regions of constitutive heterochromatin. In most organisms, constitutive heterochromatin occurs around the chromosome centromere and near telomeres.

Facultative heterochromatin

The regions of DNA packaged in facultative heterochromatin will not be consistent between the cell types within a species, and thus a sequence in one cell that is packaged in facultative heterochromatin (and the genes within are poorly expressed) may be packaged in euchromatin in another cell (and the genes within are no longer silenced). However, the formation of facultative heterochromatin is regulated, and is often associated with morphogenesis or differentiation. An example of facultative heterochromatin is X chromosome inactivation in female mammals: one X chromosome is packaged as facultative heterochromatin and silenced, while the other X chromosome is packaged as euchromatin and expressed.

Among the molecular components that appear to regulate the spreading of heterochromatin are the Polycomb-group proteins and non-coding genes such as Xist. The mechanism for such spreading is still a matter of controversy.[18] The polycomb repressive complexes PRC1 and PRC2 regulate chromatin compaction and gene expression and have a fundamental role in developmental processes. PRC-mediated epigenetic aberrations are linked to genome instability and malignancy and play a role in the DNA damage response, DNA repair and in the fidelity of replication.[19]

Yeast heterochromatin

Saccharomyces cerevisiae, or budding yeast, is a model eukaryote and its heterochromatin has been defined thoroughly. Although most of its genome can be characterized as euchromatin, S. cerevisiae has regions of DNA that are transcribed very poorly. These loci are the so-called silent mating type loci (HML and HMR), the rDNA (encoding ribosomal RNA), and the sub-telomeric regions. Fission yeast (Schizosaccharomyces pombe) uses another mechanism for heterochromatin formation at its centromeres. Gene silencing at this location depends on components of the RNAi pathway. Double-stranded RNA is believed to result in silencing of the region through a series of steps.

In the fission yeast Schizosaccharomyces pombe, two RNAi complexes, the RITS complex and the RNA-directed RNA polymerase complex (RDRC), are part of an RNAi machinery involved in the initiation, propagation and maintenance of heterochromatin assembly. These two complexes localize in a siRNA-dependent manner on chromosomes, at the site of heterochromatin assembly. RNA polymerase II synthesizes a transcript that serves as a platform to recruit RITS, RDRC and possibly other complexes required for heterochromatin assembly.[20][21] Both RNAi and an exosome-dependent RNA degradation process contribute to heterochromatic gene silencing. These mechanisms of Schizosaccharomyces pombe may occur in other eukaryotes.[22] A large RNA structure called RevCen has also been implicated in the production of siRNAs to mediate heterochromatin formation in some fission yeast.[23]

Heterochromatin vs. euchromatin
David O Morgan – The Cell Cycle. Principles of Control.
Heterochromatin contains specialized proteins (red) that bind to histone H3 or H4 subunits that have been marked by a specific modification (green). The enzyme that performs this modification is also present in heterochromatin (blue), ensuring that the modification is maintained.[1]
General model for duplication of heterochromatin during cell division
David O Morgan – The Cell Cycle. Principles of Control.
Heterochromatin contains specialized proteins (red) that bind to histone H3 or H4 subunits that have been marked by a specific modification (green). The enzyme that performs this modification is also present in heterochromatin (blue), ensuring that the modification is maintained. When the chromosome is duplicated, the marked histone H3–H4 tetramers of the parent chromosome are distributed randomly to the two daughter strands, resulting in a mixture of old (light grey) and new (dark grey) nucleosomes. In heterochromatin, new nucleosomes are rapidly marked by the histone-modifying enzymes bound to old nucleosomes. This provides new binding sites for heterochromatin proteins. These proteins (such as the Sir complex or HP1) also have the ability to bind to each other, further promoting the assembly of a protein polymer along the chromosome. It can also be seen in this diagram that the boundary between heterochromatin and euchromatin is not rigidly fixed, because small local changes in the extent of histone modification could cause shifts in its position.[1]
Microscopy of heterochromatic versus euchromatic nuclei (H&E stain).
 Mikael Häggström, M.D. – Author info – Reusing images – Conflicts of interest:   None Mikael Häggström Consent note: Consent from the patient or patient’s relatives is regarded as redundant, because of absence of identifiable features (List of HIPAA identifiers) in the media and case information (See also HIPAA case reports guidance). – Own work
Microscopy of heterochromatic versus euchromatic nuclei (H&E stain of benign squamous cells).

See also

References

  1. ^ Volpe TA, Kidner C, Hall IM, Teng G, Grewal SI, Martienssen RA (September 2002). “Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi”. Science. 297 (5588): 1833–7. Bibcode:2002Sci…297.1833V. doi:10.1126/science.1074973. PMID 12193640. S2CID 2613813.
  2. ^ “What is the current evidence showing active transcription withinin…” www.researchgate.net. Retrieved 2016-04-30.
  3. ^ Ou HD, Phan S, Deerinck TJ, Thor A, Ellisman MH, O’Shea CC (July 2017). “ChromEMT: Visualizing 3D chromatin structure and compaction in interphase and mitotic cells”. Science. 357 (6349): eaag0025. doi:10.1126/science.aag0025. PMC 5646685. PMID 28751582.
  4. ^ Oberdoerffer P, Sinclair DA (September 2007). “The role of nuclear architecture in genomic instability and ageing”. Nature Reviews. Molecular Cell Biology. 8 (9): 692–702. doi:10.1038/nrm2238. PMID 17700626. S2CID 15674132.
  5. ^ Rosenfeld JA, Wang Z, Schones DE, Zhao K, DeSalle R, Zhang MQ (March 2009). “Determination of enriched histone modifications in non-genic portions of the human genome”. BMC Genomics. 10 (1): 143. doi:10.1186/1471-2164-10-143. PMC 2667539. PMID 19335899.
  6. ^ Nicetto D, Donahue G, Jain T, Peng T, Sidoli S, Sheng L, et al. (January 2019). “H3K9me3-heterochromatin loss at protein-coding genes enables developmental lineage specification”. Science. 363 (6424): 294–297. Bibcode:2019Sci…363..294N. doi:10.1126/science.aau0583. PMC 6664818. PMID 30606806.
  7. ^ Elgin, S.C. (1996). “Heterochromatin and gene regulation in Drosophila“. Current Opinion in Genetics & Development. 6 (2): 193–202. doi:10.1016/S0959-437X(96)80050-5. ISSN 0959-437X. PMID 8722176.
  8. ^ van Steensel B (May 2011). “Chromatin: constructing the big picture”. The EMBO Journal. 30 (10): 1885–95. doi:10.1038/emboj.2011.135. PMC 3098493. PMID 21527910.
  9. ^ Roudier F, Ahmed I, Bérard C, Sarazin A, Mary-Huard T, Cortijo S, et al. (May 2011). “Integrative epigenomic mapping defines four main chromatin states in Arabidopsis”. The EMBO Journal. 30 (10): 1928–38. doi:10.1038/emboj.2011.103. PMC 3098477. PMID 21487388.
  10. ^ Lohe AR, Hilliker AJ, Roberts PA (August 1993). “Mapping simple repeated DNA sequences in heterochromatin of Drosophila melanogaster”. Genetics. 134 (4): 1149–74. doi:10.1093/genetics/134.4.1149. PMC 1205583. PMID 8375654.
  11. ^ Lu BY, Emtage PC, Duyf BJ, Hilliker AJ, Eissenberg JC (June 2000). “Heterochromatin protein 1 is required for the normal expression of two heterochromatin genes in Drosophila”. Genetics. 155 (2): 699–708. doi:10.1093/genetics/155.2.699. PMC 1461102. PMID 10835392.
  12. ^ Grewal SI, Jia S (January 2007). “Heterochromatin revisited”. Nature Reviews. Genetics. 8 (1): 35–46. doi:10.1038/nrg2008. PMID 17173056. S2CID 31811880. An up-to-date account of the current understanding of repetitive DNA, which usually doesn’t contain genetic information. If evolution makes sense only in the context of the regulatory control of genes, we propose that heterochromatin, which is the main form of chromatin in higher eukaryotes, is positioned to be a deeply effective target for evolutionary change. Future investigations into assembly, maintenance and the many other functions of heterochromatin will shed light on the processes of gene and chromosome regulation.
  13. ^ Fisher AG, Merkenschlager M (April 2002). “Gene silencing, cell fate and nuclear organisation”. Current Opinion in Genetics & Development. 12 (2): 193–7. doi:10.1016/S0959-437X(02)00286-1. PMID 11893493.
  14. ^ Zhimulev, I.F.; et al. (December 1986). “Cytogenetic and molecular aspects of position effect variegation in Drosophila melanogaster”. Chromosoma. 94 (6): 492–504. doi:10.1007/BF00292759. ISSN 1432-0886. S2CID 24439936.
  15. ^ Burgess-Beusse B, Farrell C, Gaszner M, Litt M, Mutskov V, Recillas-Targa F, et al. (December 2002). “The insulation of genes from external enhancers and silencing chromatin”. Proceedings of the National Academy of Sciences of the United States of America. 99 Suppl 4 (Suppl 4): 16433–7. Bibcode:2002PNAS…9916433B. doi:10.1073/pnas.162342499. PMC 139905. PMID 12154228.
  16. ^ Allis CD, Grewal SI (August 2001). “Transitions in distinct histone H3 methylation patterns at the heterochromatin domain boundaries”. Science. 293 (5532): 1150–5. doi:10.1126/science.1064150. PMID 11498594. S2CID 26350729.
  17. ^ Donze D, Kamakaka RT (February 2001). “RNA polymerase III and RNA polymerase II promoter complexes are heterochromatin barriers in Saccharomyces cerevisiae”. The EMBO Journal. 20 (3): 520–31. doi:10.1093/emboj/20.3.520. PMC 133458. PMID 11157758.
  18. ^ Talbert PB, Henikoff S (October 2006). “Spreading of silent chromatin: inaction at a distance”. Nature Reviews. Genetics. 7 (10): 793–803. doi:10.1038/nrg1920. PMID 16983375. S2CID 1671107.
  19. ^ Veneti Z, Gkouskou KK, Eliopoulos AG (July 2017). “Polycomb Repressor Complex 2 in Genomic Instability and Cancer”. International Journal of Molecular Sciences. 18 (8): 1657. doi:10.3390/ijms18081657. PMC 5578047. PMID 28758948.
  20. ^ Kato H, Goto DB, Martienssen RA, Urano T, Furukawa K, Murakami Y (July 2005). “RNA polymerase II is required for RNAi-dependent heterochromatin assembly”. Science. 309 (5733): 467–9. Bibcode:2005Sci…309..467K. doi:10.1126/science.1114955. PMID 15947136. S2CID 22636283.
  21. ^ Djupedal I, Portoso M, Spåhr H, Bonilla C, Gustafsson CM, Allshire RC, Ekwall K (October 2005). “RNA Pol II subunit Rpb7 promotes centromeric transcription and RNAi-directed chromatin silencing”. Genes & Development. 19 (19): 2301–6. doi:10.1101/gad.344205. PMC 1240039. PMID 16204182.
  22. ^ Vavasseur; et al. (2008). “Heterochromatin Assembly and Transcriptional Gene Silencing under the Control of Nuclear RNAi: Lessons from Fission Yeast”. RNA and the Regulation of Gene Expression: A Hidden Layer of Complexity. Caister Academic Press. ISBN 978-1-904455-25-7.
  23. ^ Djupedal I, Kos-Braun IC, Mosher RA, Söderholm N, Simmer F, Hardcastle TJ, et al. (December 2009). “Analysis of small RNA in fission yeast; centromeric siRNAs are potentially generated through a structured RNA”. The EMBO Journal. 28 (24): 3832–44. doi:10.1038/emboj.2009.351. PMC 2797062. PMID 19942857.

External links

Cytogenetics: chromosomes

Categories: 

Tags:

Leave a Reply

Your email address will not be published. Required fields are marked *

This site uses Akismet to reduce spam. Learn how your comment data is processed.