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ZW sex-determination system

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ZW sex determination in birds (as exemplified with chickens)
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The ZW sex-determination system is a chromosomal 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), the schistosome family of flatworms, and some reptiles, e.g. majority of snakes, lacertid lizards and monitors, including Komodo dragons. It is also present in some plants, where it has probably evolved independently on several occasions.[1] The letters Z and W are used to distinguish this system from the XY sex-determination system. In the ZW system, females have a pair of dissimilar ZW chromosomes, and males have two similar ZZ chromosomes.

In contrast to the XY sex-determination system and the X0 sex-determination system, where the sperm determines the sex, in the ZW system, the ovum determines the sex of the offspring. Males are the homogametic sex (ZZ), while females are the heterogametic sex (ZW). The Z chromosome is larger and has more genes, similarly to the X chromosome in the XY system.

Significance of the ZW and XY systems

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No genes are shared between the avian ZW and mammalian XY chromosomes,[2] and, from a comparison between chicken and human, the Z chromosome appears similar to the autosomal chromosome 9 in humans. It has been proposed 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.[3]

The platypus, a monotreme mammal, has a system of five pairs of XY chromosomes. They form a multiple chain due to homologous regions in male meiosis and finally segregates into XXXXX-sperm and YYYYY-sperm. The bird Z-like pair shows up on opposite ends of the chain. Areas homologous to the bird Z chromosome are scattered throughout X3 and X5.[4]: fig. 5  Although the sex-determination system is not necessarily linked to that of birds and definitely not to that of therian mammals, the similarity at least allowed for the conclusion that mammals evolved sex chromosomes twice.[5] The previous report that platypus has X chromosomes similar to that of therian mammals is now considered a mistake.[6]

Bird and snake ZW are unrelated, having evolved from different autosomes.[7] However, the bird-like chromosomes of platypus may indicate that ancestors of snakes had a bird-like ZW system.[6]

Across species

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In birds

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In 2007, a time where there had not been extensive research on other organisms with the ZW sex-determination system, researchers announced that chickens' and zebra finches' sex chromosomes do not exhibit any type of chromosome-wide dosage compensation, and instead seem to dosage compensate on a gene-by-gene basis.[8][9] 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.[10][11] 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.[12][13] Both transcriptional and translational gene-specific dosage compensation have been observed in avian sex chromosomes.[14] In addition, the involvement of sex-biased miRNAs was proposed to compensate for the presence of two Z-chromosomes in male birds.[15]

It is unknown whether it might be that the presence of the W chromosome induces female features, or whether instead it is the duplication of the Z chromosome that induces male ones; unlike mammals, no birds with a double W chromosome (ZWW) or a single Z (Z0) have been satisfactorily documented. However, it is known that the removal or damage to the ovaries of female birds can lead to the development of male plumage, suggesting that female hormones repress the expression of male characteristics in birds.[16] It appears possible that either condition could cause embryonic death, or that both chromosomes could be responsible for sex selection.[17][better source needed] 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.[14][18]

The ZW sex-determination system makes it possible to create sex-link chickens in which color at hatching is differentiated by sex, thus making chick-sexing an easier process.

In snakes

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Snakes' W chromosomes show different levels of decay compared to their Z chromosomes. This allows for tracking the shrinking of W chromosomes (analogous to the shrinking of Y chromosomes) by comparing across species. Mapping of specific genes reveals that the snake system is different from the bird system. It is not yet known which gene is the sex-determining one in snakes. One thing that stood out was that pythons show little signs of "W-shrinking".[7]

Boa and Python families are now known to probably have an XY sex-determination system.[19] Interest in looking into this came from female family members capable of parthenogenesis, or producing offspring without mating. In 2010 a female Boa constrictor that produced 22 female offspring in this manner was found in the wild. By then it was presumed that such a pattern was produced by WW chromosomes.[20] Python bivittatus and Boa imperator, similarly only produce female offspring; their genomes share male-specific single nucleotide polymorphisms identifiable by restriction enzyme digestion. Their chromosomal origins, however, differ: Python's XY are similar to other snakes' ZW, while Boa XY maps to microchromosomes in other snakes.[21] The female-only pattern is in contrast to the ZW Colubroidean parthenogens, which always produce male (ZZ) offspring.[22]

In moths and butterflies

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In Lepidoptera (moths and butterflies), females can have Z, ZZW, or ZZWW.[23]

In schistosomes

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The family Schistosomatidae, commonly called blood flukes, are small parasitic flatworms dwelling in the blood vessels of the bladder, liver, intestines and other organs of birds and mammals. They are the only sexually heteromorphic family among the trematode class, and depend on remaining biochemically paired in copula to complete their life cycle.[24] The heterogametic sex chromosomes in females of nine species of schistosomes were first described by geneticist Margaret Menzel and parasitologist Robert B. Short of Florida State University in 1960.[25][26] The difference in the sex chromosomes was noted during the pachytene stage of meiotic prophase.

In turtles

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Trionychidae turtles possess a ZZ-ZW sex determinate system, which originated sometime between the beginning of the Jurassic and the Early Cretaceous.[27]

In plants

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Among the approximately 5% of plant species that have separate male and female individuals (dioecious), several are known to have a ZW system of sex determination. These include pistachio, several species of strawberry such as Fragaria virginiana and Fragaria chiloensis, and several species of willow including Salix viminalis and Salix purpurea.[1][28]

See also

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References

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  1. ^ a b Zhou, Ran; Macaya-Sanz, David; Carlson, Craig H.; thirteen others, and (14 February 2020). "A willow sex chromosome reveals convergent evolution of complex palindromic repeats". Genome Biology. 21 (1): 38. doi:10.1186/s13059-020-1952-4. PMC 7023750. PMID 32059685.
  2. ^ 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. S2CID 12932564.
  3. ^ Ellegren, Hans (1 March 2011). "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. PMID 21301475. S2CID 21098648.
  4. ^ Deakin, JE; Graves, JA; Rens, W (2012). "The evolution of marsupial and monotreme chromosomes". Cytogenetic and Genome Research. 137 (2–4): 113–29. doi:10.1159/000339433. hdl:1885/64794. PMID 22777195.
  5. ^ Cortez, Diego; Marin, Ray; Toledo-Flores, Deborah; Froidevaux, Laure; Liechti, Angélica; Waters, Paul D.; Grützner, Frank; Kaessmann, Henrik (24 April 2014). "Origins and functional evolution of Y chromosomes across mammals". Nature. 508 (7497): 488–493. Bibcode:2014Natur.508..488C. doi:10.1038/nature13151. PMID 24759410. S2CID 4462870.
  6. ^ a b Veyrunes F, Waters PD, Miethke P, et al. (2008). "Bird-like sex chromosomes of platypus imply recent origin of mammal sex chromosomes". Genome Research. 18 (6): 965–973. doi:10.1101/gr.7101908. PMC 2413164. PMID 18463302.
  7. ^ a b Matsubara, K; Tarui, H; Toriba, M; Yamada, K; Nishida-Umehara, C; Agata, K; Matsuda, Y (28 November 2006). "Evidence for different origin of sex chromosomes in snakes, birds, and mammals and step-wise differentiation of snake sex chromosomes". Proceedings of the National Academy of Sciences of the United States of America. 103 (48): 18190–5. doi:10.1073/pnas.0605274103. PMC 1838728. PMID 17110446.
  8. ^ Ellegren, Hans; Hultin-Rosenberg, Lina; Brunström, Björn; Dencker, Lennart; Kultima, Kim; Scholz, Birger (20 September 2007). "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.
  9. ^ Itoh, Yuichiro; Melamed, Esther; Yang, Xia; Kampf, Kathy; Wang, Susanna; Yehya, Nadir; Van Nas, Atila; Replogle, Kirstin; Band, Mark R. (1 January 2007). "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.
  10. ^ Mank, J. E.; Ellegren, H. (1 March 2009). "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.
  11. ^ Mank, Judith E.; Hosken, David J.; Wedell, Nina (1 August 2011). "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. PMID 21790564. S2CID 43470911.
  12. ^ Wolf, Jochen BW; Bryk, Jarosław (1 February 2011). "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.
  13. ^ Adolfsson, Sofia; Ellegren, Hans (1 April 2013). "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.
  14. ^ a b Uebbing, Severin; Konzer, Anne; Xu, Luohao; Backström, Niclas; Brunström, Björn; Bergquist, Jonas; Ellegren, Hans (24 June 2015). "Quantitative Mass Spectrometry Reveals Partial Translational Regulation for Dosage Compensation in Chicken". Molecular Biology and Evolution. 32 (10): 2716–25. doi:10.1093/molbev/msv147. ISSN 0737-4038. PMC 4576709. PMID 26108680.
  15. ^ Warnefors, Maria; Mössinger, Katharina; Halbert, Jean; Studer, Tania; VandeBerg, John L.; Lindgren, Isa; Fallahshahroudi, Amir; Jensen, Per; Kaessmann, Henrik (27 October 2017). "Sex-biased microRNA expression in mammals and birds reveals underlying regulatory mechanisms and a role in dosage compensation". Genome Research. 27 (12): 1961–1973. doi:10.1101/gr.225391.117. PMC 5741053. PMID 29079676.
  16. ^ Graves, J. a. M. (2003). "Sex and death in birds: a model of dosage compensation that predicts lethality of sex chromosome aneuploids". Cytogenetic and Genome Research. 101 (3–4): 278–282. doi:10.1159/000074349. ISSN 1424-859X. PMID 14684995. S2CID 24824551. Archived from the original on 26 October 2020. Retrieved 21 October 2020.
  17. ^ 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. S2CID 16436279.
  18. ^ Naurin, Sara; Hansson, Bengt; Bensch, Staffan; Hasselquist, Dennis (1 January 2010). "Why does dosage compensation differ between XY and ZW taxa?". Trends in Genetics. 26 (1): 15–20. doi:10.1016/j.tig.2009.11.006. ISSN 0168-9525. PMID 19963300.
  19. ^ Emerson, J.J. (August 2017). "Evolution: A Paradigm Shift in Snake Sex Chromosome Genetics". Current Biology. 27 (16): R800–R803. Bibcode:2017CBio...27.R800E. doi:10.1016/j.cub.2017.06.079. PMID 28829965.
  20. ^ "Boa constrictor produces fatherless babies". CBC News. 3 November 2010. Archived from the original on 17 February 2021. Retrieved 3 November 2010.
  21. ^ Gamble, Tony; Castoe, Todd A.; Nielsen, Stuart V.; Banks, Jaison L.; Card, Daren C.; Schield, Drew R.; Schuett, Gordon W.; Booth, Warren (24 July 2017). "The Discovery of XY Sex Chromosomes in a Boa and Python". Current Biology. 27 (14): 2148–2153.e4. Bibcode:2017CBio...27E2148G. doi:10.1016/j.cub.2017.06.010. ISSN 1879-0445. PMID 28690112. Archived from the original on 28 April 2019. Retrieved 24 January 2019.
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  23. ^ Majerus ME (2003). Sex Wars: Genes, Bacteria, and Biased Sex Ratios. Princeton University Press. p. 59. ISBN 978-0-691-00981-0.
  24. ^ Atkinson, Kristine H.; Atkinson, Burr G. (31 January 1980). "Biochemical basis for the continuous copulation of female Schistosoma mansoni". Nature. 118 (2): 478–479. Bibcode:1980Natur.283..478A. doi:10.1038/283478a0. PMID 7352026. S2CID 4337699.
  25. ^ Menzel, Margaret Y.; Short, Robert B. (1960). "Pachytene chromosomes in three species of schistosomes: sex and autosomal bivalents in males and females". Journal of Heredity. 51 (1): 3–12. doi:10.1093/oxfordjournals.jhered.a106943.
  26. ^ Short, Robert B.; Menzel, Margaret Y. (1960). "Chromosomes of nine species of schistosomes". Journal of Parasitology. 46 (3): 273–287. doi:10.2307/3275488. JSTOR 3275488. PMID 14446186.
  27. ^ Rovatsos, Michail; Praschag, Peter; Fritz, Uwe; Kratochvšl, Lukáš (10 February 2017). "Stable Cretaceous sex chromosomes enable molecular sexing in softshell turtles (Testudines: Trionychidae)". Scientific Reports. 7 (1): 42150. Bibcode:2017NatSR...742150R. doi:10.1038/srep42150. ISSN 2045-2322. PMC 5301483. PMID 28186115.
  28. ^ Charlesworth, Deborah (2015). "Plant Sex Chromosomes". Annual Review of Plant Biology. 67: 397–420. doi:10.1146/annurev-arplant-043015-111911. PMID 26653795. Archived from the original on 24 April 2021. Retrieved 8 December 2020.

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