The nucleus of a human cell showing the location of heterochromatin

Heterochromatin is a tightly packed form of DNA, which comes in multiple varieties. These varieties lie on a continuum between the two extremes of constitutive 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).

Constitutive heterochromatin can affect the genes near itself (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.[3]

Heterochromatin has been associated with the di- and tri-methylation of H3K9 in certain portions of the genome.[4]


Chromatin is found in two varieties: euchromatin and heterochromatin.[5] Originally, the two forms were distinguished cytologically by how intensely they 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[6] and plants[7] 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,[8] and many genes are repressed to various extents, although some cannot be expressed in euchromatin at all.[9] Both centromeres and telomeres are heterochromatic, as is the Barr body of the second, inactivated X-chromosome in a female.


Heterochromatin has been associated with several functions, from gene regulation to the protection of chromosome integrity;[10] 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,[11] which may be demonstrated by position-effect variegation.[12] 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,[13] and loci in two Saccharomyces spp.[14][15]).

Constitutive heterochromatin

All cells of a given species that 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.[16]

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.[17][18] Both RNAi and an exosome-dependent RNA degradation process contribute to heterochromatic gene silencing. These mechanisms of Schizosaccharomyces pombe may occur in other eukaryotes.[19] A large RNA structure called RevCen has also been implicated in the production of siRNAs to mediate heterochromatin formation in some fission yeast.[20]

See also


  1. Volpe, Thomas A.; Kidner, Catherine; Hall, Ira M.; Teng, Grace; Grewal, Shiv I. S.; Martienssen, Robert A. (2002-09-13). "Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi". Science (New York, N.Y.). 297 (5588): 1833–1837. doi:10.1126/science.1074973. ISSN 1095-9203. PMID 12193640.
  2. "What is the current evidence showing active transcription withinin...". www.researchgate.net. Retrieved 2016-04-30.
  3. Oberdoerffer, P; Sinclair, D (2007). "The role of nuclear architecture in genomic instability and ageing". Nature Reviews Molecular Cell Biology. 8: 692–702. doi:10.1038/nrm2238.
  4. Rosenfeld, Jeffrey A; Wang, Zhibin; Schones, Dustin; Zhao, Keji; Desalle, Rob; Zhang, Michael Q (31 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 2667539Freely accessible. PMID 19335899.
  5. 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.
  6. van Steensel, B. (2011). "Chromatin: constructing the big picture". The EMBO Journal. 30 (10): 1885–95. doi:10.1038/emboj.2011.135. PMC 3098493Freely accessible. PMID 21527910.
  7. Roudier, François; et al. (2011). "Integrative epigenomic mapping defines four main chromatin states in Arabidopsis". The EMBO Journal. 30 (10): 1928–1938. doi:10.1038/emboj.2011.103. PMC 3098477Freely accessible. PMID 21487388.
  8. Lohe, A.R.; et al. (August 1, 1993). "Mapping Simple Repeated DNA Sequences in Heterochromatin of Drosophila Melanogaster". Genetics. 134 (4): 1149–74. ISSN 0016-6731. PMC 1205583Freely accessible. PMID 8375654.
  9. Lu, B.Y.; et al. (June 1, 2000). "Heterochromatin protein 1 is required for the normal expression of two heterochromatin genes in Drosophila". Genetics. 155 (2): 699–708. ISSN 0016-6731. PMC 1461102Freely accessible. PMID 10835392.
  10. Grewal SI, Jia S (January 2007). "Heterochromatin revisited". Nature Reviews Genetics. 8 (1): 35–. doi:10.1038/nrg2008. PMID 17173056. Retrieved 18 September 2013. 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.
  11. Fisher, Amanda G.; Matthias Merkenschlager (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. ISSN 0959-437X. PMID 11893493.
  12. 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.
  13. Burgess-Beusse, B; et al. (December 2002). "The insulation of genes from external enhancers and silencing chromatin". Proc. Natl. Acad. Sci. USA. 9 (Suppl 4): 16433–7. doi:10.1073/pnas.162342499. PMC 139905Freely accessible. PMID 12154228.
  14. Noma, K.; et al. (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.
  15. Donze, D.; R.T. Kamakaka (2000). "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 133458Freely accessible. PMID 11157758.
  16. 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.
  17. Kato, H.; et al. (2005). "RNA Polymerase II Is Required for RNAi-Dependent Heterochromatin Assembly". Science. 309: 467–469. doi:10.1126/science.1114955.
  18. Djupedal, I.; et al. (2005). "RNA Pol II subunit Rpb7 promotes centromeric transcription and RNAi-directed chromatin silencing". Genes & Development. 19: 2301–2306. doi:10.1101/gad.344205.
  19. 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.
  20. Djupedal I, Kos-Braun IC, Mosher RA, et al. (December 2009). "Analysis of small RNA in fission yeast; centromeric siRNAs are potentially generated through a structured RNA". EMBO J. 28 (24): 3832–44. doi:10.1038/emboj.2009.351. PMC 2797062Freely accessible. PMID 19942857.
This article is issued from Wikipedia - version of the 11/8/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.