Long-term stability of sex chromosome gene content allows accurate qPCR-based molecular sexing across birds
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081766%3A_____%2F21%3A00541789" target="_blank" >RIV/68081766:_____/21:00541789 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11310/21:10434241
Result on the web
<a href="https://onlinelibrary.wiley.com/doi/10.1111/1755-0998.13381" target="_blank" >https://onlinelibrary.wiley.com/doi/10.1111/1755-0998.13381</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1111/1755-0998.13381" target="_blank" >10.1111/1755-0998.13381</a>
Alternative languages
Result language
angličtina
Original language name
Long-term stability of sex chromosome gene content allows accurate qPCR-based molecular sexing across birds
Original language description
Embryos, juveniles, and even adults of many bird species lack pronounced external sexually dimorphic characteristics. Accurate identification of sex is crucial for research (e.g., developmental, population, and evolutionary studies), management of wildlife species, and captive breeding programmes for both conservation and poultry. An accurate molecular sexing method applicable across the entire bird radiation is theoretically possible thanks to the long-term stability of their ZZ/ZW sex chromosomes, but current methods are not applicable in a wide range of bird lineages. Here, we developed a novel molecular sexing method based on the comparison of gene copy number variation by quantitative real-time PCR (qPCR) in conserved Z-specific genes (CHRNA6, DDX4, LPAR1, TMEM161B, VPS13A), i.e. genes linked to Z but absent from W chromosomes. We tested the method across three paleognath and 70 neognath species covering the avian phylogeny. In addition, we designed primers for four Z-specific genes (DOCK8, FUT10, PIGG and PSD3) for qPCR-based molecular sexing in three paleognath species. We have demonstrated that the genes DOCK8, FUT10, PIGG and PSD3 can identify sex in paleognath birds and the genes CHRNA6, DDX4, TMEM161B, and VPS13A can reveal sex in neognath birds. The gene LPAR1 can be used to accurately identify sex in both paleognath and neognath species. Along with outlining a novel method of practical importance for molecular sexing in birds, our study also documents in detail the conservation of sex chromosomes across the avian phylogeny.
Czech name
—
Czech description
—
Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
10602 - Biology (theoretical, mathematical, thermal, cryobiology, biological rhythm), Evolutionary biology
Result continuities
Project
<a href="/en/project/GA18-15020S" target="_blank" >GA18-15020S: Evolution of brain complexity and processing capacity in amphibians and reptiles: A quantitative approach to understanding tetrapod brain evolution</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2021
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Molecular Ecology Resources
ISSN
1755-098X
e-ISSN
1755-0998
Volume of the periodical
21
Issue of the periodical within the volume
6
Country of publishing house
GB - UNITED KINGDOM
Number of pages
9
Pages from-to
2013-2021
UT code for WoS article
000635932300001
EID of the result in the Scopus database
2-s2.0-85103984148