Sex-chromosome dosage compensation

Dosage compensation is the process by which organisms equalize the expression of genes between members of different biological sexes. Across species, different sexes are often characterized by different types and numbers of sex chromosomes. In order to neutralize the large difference in gene dosage produced by differing numbers of sex chromosomes among the sexes, various evolutionary branches have acquired various methods to equalize gene expression among the sexes. Because sex chromosomes contain different numbers of genes, different species of organisms have developed different mechanisms to cope with this inequality. Replicating the actual gene is impossible; thus organisms instead equalize the expression from each gene. For example, in humans, female (XX) cells randomly silence the transcription of one X chromosome, and transcribe all information from the other, expressed X chromosome. Thus, human females have the same number of expressed X-linked genes per cell as do human males (XY), both sexes having essentially one X chromosome per cell, from which to transcribe and express genes.[1]

Different lineages have evolved different mechanisms to cope with the differences in gene copy numbers between the sexes that are observed on sex chromosomes. Some lineages have evolved dosage compensation, an epigenetic mechanism which restores expression of X or Z specific genes in the heterogametic sex to the same levels observed in the ancestor prior to the evolution of the sex chromosome.[2][3] Other lineages equalize the expression of the X- or Z- specific genes between the sexes, but not to the ancestral levels, i.e. they possess incomplete compensation with "dosage balance". One example of this is X-inactivation which occurs in humans. The third documented type of gene dose regulatory mechanism is incomplete compensation without balance (sometimes referred to as incomplete or partial dosage compensation). In this system gene expression of sex-specific loci is reduced in the heterogametic sex i.e. the females in ZZ/ZW systems and males in XX/XY systems.[4]

There are three main mechanisms of achieving dosage compensation which are widely documented in the literature and which are common to most species. These include random inactivation of one female X chromosome (as observed in humans and Mus musculus; this is called X-inactivation), a two-fold increase in the transcription of a single male X chromosome (as observed in Drosophila melanogaster), and decreased transcription by half in both of the X chromosomes of a hermaphroditic organism (as observed in Caenorhabditis elegans). These mechanisms have been widely studied and manipulated in model organisms commonly used in the laboratory research setting. A summary of these forms of dosage compensation is illustrated below. However, there are also other less common forms of dosage compensation, which are not as widely researched and are sometimes specific to only one species (as observed in certain bird and monotreme species).

Three main mechanisms of dosage compensation observed in common model eukaryotic organisms.
  1. ^ Brockdorff, N.; Turner, B.M. (2015). "Dosage compensation in mammals". Cold Spring Harbor Perspectives in Biology. 7 (3): a019406. doi:10.1101/cshperspect.a019406. PMC 4355265. PMID 25731764.
  2. ^ Ohno, S (1967). Sex chromosomes and sex linked genes. Springer verlag.
  3. ^ Höglund, Andrey; Henriksen, Rie; Churcher, Allison M.; Guerrero-Bosagna, Carlos M.; Martinez-Barrio, Alvaro; Johnsson, Martin; Jensen, Per; Wright, Dominic (2024-03-08). Van Oers, Kees (ed.). "The regulation of methylation on the Z chromosome and the identification of multiple novel Male Hyper-Methylated regions in the chicken". PLOS Genetics. 20 (3): e1010719. doi:10.1371/journal.pgen.1010719. ISSN 1553-7404. PMC 10954189. PMID 38457441.
  4. ^ Teranishi, Mika; Shimada, Yukiko; Hori, Tetsuya; Nakabayashi, Osamu; Kikuchi, Tateki; Macleod, Tracy; Pym, Robert; Sheldon, Bruce; Solovei, Irina; Macgregor, Herbert; Mizuno, Shigeki (2001). "Transcripts of the MHM region on the chicken Z chromosome accumulate as non-coding RNA in the nucleus of female cells adjacent to the DMRT1 locus". Chromosome Research. 9 (2): 147–165. doi:10.1023/A:1009235120741.