ZW sex-determination system

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ZW sex determination in birds (as exemplified with chickens)

The ZW sex-determination system is a system that determines the sex of offspring in birds, some fish and crustaceans such as the giant river prawn, some insects (including butterflies and moths), and some reptiles, including Komodo dragons. In the ZW system, the ovum determines the sex of the offspring, in contrast to the XY sex-determination system and the X0 sex-determination system, wherein the sperm determines the sex. The letters Z and W are used to distinguish this system from the XY system. Males are the homogametic sex (ZZ), while females are the heterogametic sex (ZW). The Z chromosome is larger and has more genes, like the X chromosome in the XY system.

While there has not been extensive research on other organisms with the ZW sex-determination system, in 2007, researchers announced that chicken and zebra finch's sex chromosomes do not exhibit any type of chromosome-wide dosage compensation and instead seem to dosage compensate on a gene-by-gene basis.[1][2] Specific locations on the chicken Z chromosome, such as the MHM region, are thought to exhibit regional dosage compensation, though researchers have argued that this region does not actually constitute local dosage compensation.[3][4] Further research expanded the list of birds that do not exhibit any type of chromosome-wide dosage compensation to crows and ratites, thus implying that all avian chromosomes lack chromosome-wide dosage compensation.[5][6] Both transcriptional and translational gene-specific dosage compensation have been observed in avian sex chromosomes.[7]

On November 3, 2010, scientists announced the discovery of a female Boa constrictor that can produce offspring without mating and, through such asexual reproduction, produced 22 female offspring, all with a WW chromosome genetic makeup. Although this result has been achieved in laboratory settings previously, never before has it been witnessed under natural circumstances. It is not clear as to whether the all-female snake neonates will eventually mate with a male, or reproduce asexually, or do both as does their mother. However, because of their WW chromosomes, any offspring they produce will be female.[8]

It is unknown whether the presence of the W chromosome induces female features or the duplication of the Z chromosome induces male ones; unlike mammals, no birds with a double W chromosome (ZWW) or a single Z (Z0) have been discovered. It appears possible that either condition could cause embryonic death, or that both chromosomes could be responsible for sex selection.[9] One possible gene that could determine sex in birds is the DMRT1 gene. Studies have shown that two copies of the gene are necessary for male sex determination.[7][10]

In Lepidoptera (moths and butterflies), examples of Z0, ZZW, and ZZWW females can be found. This suggests that the W chromosome is essential in female determination in some species (ZZW), but not in others (Z0). In Bombyx mori (the commercial silkworm), the W chromosome carries the female-determining genes.

No genes are shared between the avian ZW and mammalian XY chromosomes,[11] and, from a comparison between chicken and human, the Z chromosome appeared similar to the autosomal chromosome 9 in humans, rather than X or Y, leading researchers to believe that the ZW and XY sex determination systems do not share an origin, but that the sex chromosomes are derived from autosomal chromosomes of the common ancestor. These autosomes are thought to have evolved sex-determining loci that eventually developed into the respective sex chromosomes once the recombination between the chromosomes (X and Y or Z and W) was suppressed.[12] A paper from 2004 compared the chicken Z chromosome with platypus X chromosomes and suggested that the two systems are related.[13] The platypus has a ten-chromosome–based system, where the chromosomes form a multivalent chain in male meiosis, segregating into XXXXX-sperm and YYYYY-sperm, with XY-equivalent chromosomes at one end of this chain and the ZW-equivalent chromosomes at the other end.[13]

See also[edit]


  1. ^ Ellegren, Hans; Hultin-Rosenberg, Lina; Brunström, Björn; Dencker, Lennart; Kultima, Kim; Scholz, Birger (2007-09-20). "Faced with inequality: chicken do not have a general dosage compensation of sex-linked genes". BMC Biology 5 (1): 40. doi:10.1186/1741-7007-5-40. ISSN 1741-7007. PMC 2099419. PMID 17883843. 
  2. ^ Itoh, Yuichiro; Melamed, Esther; Yang, Xia; Kampf, Kathy; Wang, Susanna; Yehya, Nadir; Van Nas, Atila; Replogle, Kirstin; Band, Mark R. (2007-01-01). "Dosage compensation is less effective in birds than in mammals". Journal of Biology 6 (1): 2. doi:10.1186/jbiol53. ISSN 1475-4924. PMC 2373894. PMID 17352797. 
  3. ^ Mank, J. E.; Ellegren, H. (2009-03-01). "All dosage compensation is local: gene-by-gene regulation of sex-biased expression on the chicken Z chromosome". Heredity 102 (3): 312–320. doi:10.1038/hdy.2008.116. ISSN 1365-2540. PMID 18985062. 
  4. ^ Mank, Judith E.; Hosken, David J.; Wedell, Nina (2011-08-01). "Some Inconvenient Truths About Sex Chromosome Dosage Compensation and the Potential Role of Sexual Conflict". Evolution 65 (8): 2133–2144. doi:10.1111/j.1558-5646.2011.01316.x. ISSN 1558-5646. 
  5. ^ Wolf, Jochen BW; Bryk, Jarosław (2011-02-01). "General lack of global dosage compensation in ZZ/ZW systems? Broadening the perspective with RNA-seq". BMC Genomics 12 (1): 91. doi:10.1186/1471-2164-12-91. ISSN 1471-2164. PMC 3040151. PMID 21284834. 
  6. ^ Adolfsson, Sofia; Ellegren, Hans (2013-04-01). "Lack of Dosage Compensation Accompanies the Arrested Stage of Sex Chromosome Evolution in Ostriches". Molecular Biology and Evolution 30 (4): 806–810. doi:10.1093/molbev/mst009. ISSN 0737-4038. PMC 3603317. PMID 23329687. 
  7. ^ a b Uebbing, Severin; Konzer, Anne; Xu, Luohao; Backström, Niclas; Brunström, Björn; Bergquist, Jonas; Ellegren, Hans (2015-06-24). "Quantitative Mass Spectrometry Reveals Partial Translational Regulation for Dosage Compensation in Chicken". Molecular Biology and Evolution: msv147. doi:10.1093/molbev/msv147. ISSN 0737-4038. PMC 4576709. PMID 26108680. 
  8. ^ "Boa constrictor produces fatherless babies". CBC News. November 3, 2010. 
  9. ^ Smith CA, Roeszler KN, Hudson QJ, Sinclair AH (2007). "Avian sex determination: what, when and where?". Cytogenet. Genome Res. 117 (1–4): 165–73. doi:10.1159/000103177. PMID 17675857. 
  10. ^ Naurin, Sara; Hansson, Bengt; Bensch, Staffan; Hasselquist, Dennis (2010-01-01). "Why does dosage compensation differ between XY and ZW taxa?". Trends in genetics: TIG 26 (1): 15–20. doi:10.1016/j.tig.2009.11.006. ISSN 0168-9525. PMID 19963300. 
  11. ^ Stiglec R, Ezaz T, Graves JA (2007). "A new look at the evolution of avian sex chromosomes". Cytogenet. Genome Res. 117 (1–4): 103–9. doi:10.1159/000103170. PMID 17675850. 
  12. ^ Ellegren, Hans (2011-03-01). "Sex-chromosome evolution: recent progress and the influence of male and female heterogamety". Nature Reviews Genetics 12 (3): 157–166. doi:10.1038/nrg2948. ISSN 1471-0056. 
  13. ^ a b Grützner, F.; Rens, W.; Tsend-Ayush, E.; El-Mogharbel, N.; O'Brien, P.C.M.; Jones, R.C.; Ferguson-Smith, M.A.; Marshall, J.A. (2004). "In the platypus a meiotic chain of ten sex chromosomes shares genes with the avian Z and mammalian X chromosomes". Nature 432 (7019): 913–917. doi:10.1038/nature03021. PMID 15502814.