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      Primary sex determination in birds depends on DMRT1 dosage, but gonadal sex does not determine adult secondary sex characteristics

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          Significance

          Here, we show that DMRT1 dosage is the key sex determination factor in birds and is essential for testis development. Furthermore, we provide additional evidence that birds, in contrast to mammals, have acquired cell-autonomous sex identity (CASI) and that the sex hormone environment does not significantly influence avian secondary sexual characteristics. This finding highlights an evolutionary divide between mammals and nonmammalian vertebrates. In mammals, the sex chromosomes determine the type of gonad formed, and sex hormones largely define the secondary sexual phenotype. In birds, the sexual phenotype is directly determined by the sex chromosome content of individual cells in different tissues. Our findings help advance our understanding of the evolution of sex determination systems and the nature of sex identity.

          Abstract

          In birds, males are the homogametic sex (ZZ) and females the heterogametic sex (ZW). Primary sex determination is thought to depend on a sex chromosome gene dosage mechanism, and the most likely sex determinant is the Z chromosome gene Doublesex and Mab-3–Related Transcription factor 1 (DMRT1). To clarify this issue, we used a CRISPR-Cas9–based monoallelic targeting approach and sterile surrogate hosts to generate birds with targeted mutations in the DMRT1 gene. The resulting chromosomally male (ZZ) chicken with a single functional copy of DMRT1 developed ovaries in place of testes, demonstrating the avian sex-determining mechanism is based on DMRT1 dosage. These ZZ ovaries expressed typical female markers and showed clear evidence of follicular development. However, these ZZ adult birds with an ovary in place of testes were indistinguishable in appearance to wild-type adult males, supporting the concept of cell-autonomous sex identity (CASI) in birds. In experiments where estrogen synthesis was blocked in control ZW embryos, the resulting gonads developed as testes. In contrast, if estrogen synthesis was blocked in ZW embryos that lacked DMRT1, the gonads invariably adopted an ovarian fate. Our analysis shows that DMRT1 is the key sex determination switch in birds and that it is essential for testis development, but that production of estrogen is also a key factor in primary sex determination in chickens, and that this production is linked to DMRT1 expression.

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          Most cited references43

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          Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

          The two most commonly used methods to analyze data from real-time, quantitative PCR experiments are absolute quantification and relative quantification. Absolute quantification determines the input copy number, usually by relating the PCR signal to a standard curve. Relative quantification relates the PCR signal of the target transcript in a treatment group to that of another sample such as an untreated control. The 2(-Delta Delta C(T)) method is a convenient way to analyze the relative changes in gene expression from real-time quantitative PCR experiments. The purpose of this report is to present the derivation, assumptions, and applications of the 2(-Delta Delta C(T)) method. In addition, we present the derivation and applications of two variations of the 2(-Delta Delta C(T)) method that may be useful in the analysis of real-time, quantitative PCR data. Copyright 2001 Elsevier Science (USA).
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            The avian Z-linked gene DMRT1 is required for male sex determination in the chicken.

            Sex in birds is chromosomally based, as in mammals, but the sex chromosomes are different and the mechanism of avian sex determination has been a long-standing mystery. In the chicken and all other birds, the homogametic sex is male (ZZ) and the heterogametic sex is female (ZW). Two hypotheses have been proposed for the mechanism of avian sex determination. The W (female) chromosome may carry a dominant-acting ovary determinant. Alternatively, the dosage of a Z-linked gene may mediate sex determination, two doses being required for male development (ZZ). A strong candidate avian sex-determinant under the dosage hypothesis is the conserved Z-linked gene, DMRT1 (doublesex and mab-3-related transcription factor 1). Here we used RNA interference (RNAi) to knock down DMRT1 in early chicken embryos. Reduction of DMRT1 protein expression in ovo leads to feminization of the embryonic gonads in genetically male (ZZ) embryos. Affected males show partial sex reversal, characterized by feminization of the gonads. The feminized left gonad shows female-like histology, disorganized testis cords and a decline in the testicular marker, SOX9. The ovarian marker, aromatase, is ectopically activated. The feminized right gonad shows a more variable loss of DMRT1 and ectopic aromatase activation, suggesting differential sensitivity to DMRT1 between left and right gonads. Germ cells also show a female pattern of distribution in the feminized male gonads. These results indicate that DMRT1 is required for testis determination in the chicken. Our data support the Z dosage hypothesis for avian sex determination.
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              A W-linked DM-domain gene, DM-W, participates in primary ovary development in Xenopus laevis.

              In the XX/XY sex-determining system, the Y-linked SRY genes of most mammals and the DMY/Dmrt1bY genes of the teleost fish medaka have been characterized as sex-determining genes that trigger formation of the testis. However, the molecular mechanism of the ZZ/ZW-type system in vertebrates, including the clawed frog Xenopus laevis, is unknown. Here, we isolated an X. laevis female genome-specific DM-domain gene, DM-W, and obtained molecular evidence of a W-chromosome in this species. The DNA-binding domain of DM-W showed a strikingly high identity (89%) with that of DMRT1, but it had no significant sequence similarity with the transactivation domain of DMRT1. In nonmammalian vertebrates, DMRT1 expression is connected to testis formation. We found DMRT1 or DM-W to be expressed exclusively in the primordial gonads of both ZZ and ZW or ZW tadpoles, respectively. Although DMRT1 showed continued expression after sex determination, DM-W was expressed transiently during sex determination. Interestingly, DM-W mRNA was more abundant than DMRT1 mRNA in the primordial gonads of ZW tadpoles early in sex determination. To assess the role of DM-W, we produced transgenic tadpoles carrying a DM-W expression vector driven by approximately 3 kb of the 5'-flanking sequence of DM-W or by the cytomegalovirus promoter. Importantly, some developing gonads of ZZ transgenic tadpoles showed ovarian cavities and primary oocytes with both drivers, suggesting that DM-W is crucial for primary ovary formation. Taken together, these results suggest that DM-W is a likely sex (ovary)-determining gene in X. laevis.
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                Author and article information

                Journal
                Proc Natl Acad Sci U S A
                Proc Natl Acad Sci U S A
                pnas
                pnas
                PNAS
                Proceedings of the National Academy of Sciences of the United States of America
                National Academy of Sciences
                0027-8424
                1091-6490
                09 March 2021
                03 March 2021
                03 March 2021
                : 118
                : 10
                : e2020909118
                Affiliations
                [1] aDivision of Functional Genomics and Development, The Roslin Institute, Royal (Dick) School of Veterinary Studies , EH25 9RG Midlothian, United Kingdom;
                [2] bLaboratory of Stem Cell Biology and Developmental Genetics, The Francis Crick Institute , NW1 1AT London, United Kingdom;
                [3] cCollege of Animal Science and Technology, Yangzhou University , 225009 Yangzhou, People's Republic of China
                Author notes
                2To whom correspondence may be addressed. Email: jason.ioannidis@ 123456roslin.ed.ac.uk or mike.mcgrew@ 123456roslin.ed.ac.uk .

                Edited by Scott V. Edwards, Harvard University, Cambridge, MA, and approved January 11, 2021 (received for review October 12, 2020)

                Author contributions: J.I., G.T., D.Z., D.G., R.L.-B., S.G., M.J.M., and M.C. designed research; J.I., G.T., D.Z., and L.L. performed research; A.I.-A. contributed new reagents/analytic tools; J.I., G.T., D.Z., and L.L. analyzed data; and J.I., G.T., D.Z., L.L., D.G., A.I.-A., R.L.-B., S.G., M.J.M., and M.C. wrote the paper.

                1J.I. and G.T. contributed equally to this work.

                3S.G., M.J.M., and M.C. contributed equally to this work.

                Author information
                https://orcid.org/0000-0003-1628-4928
                https://orcid.org/0000-0003-0579-9416
                https://orcid.org/0000-0003-0875-060X
                https://orcid.org/0000-0002-0936-1860
                https://orcid.org/0000-0001-9364-4179
                https://orcid.org/0000-0002-4920-7745
                https://orcid.org/0000-0001-8213-4632
                Article
                202020909
                10.1073/pnas.2020909118
                7958228
                33658372
                7ef3d06e-433c-42fc-ab3a-e10b99e274e9
                Copyright © 2021 the Author(s). Published by PNAS.

                This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY).

                History
                Page count
                Pages: 10
                Funding
                Funded by: RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) 501100000268
                Award ID: BB/N018672/1
                Award Recipient : Debiao Zhao Award Recipient : Robin Lovell-Badge Award Recipient : Silvana Guioli Award Recipient : Mike J McGrew Award Recipient : Michael Clinton
                Funded by: RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) 501100000268
                Award ID: FC001107
                Award Recipient : Debiao Zhao Award Recipient : Robin Lovell-Badge Award Recipient : Silvana Guioli Award Recipient : Mike J McGrew Award Recipient : Michael Clinton
                Funded by: RCUK | Medical Research Council (MRC) 501100000265
                Award ID: FC001107
                Award Recipient : Robin Lovell-Badge
                Funded by: Wellcome 100010269
                Award ID: FC001107
                Award Recipient : Robin Lovell-Badge
                Funded by: RCUK | Medical Research Council (MRC) 501100000265
                Award ID: U117512772
                Award Recipient : Robin Lovell-Badge
                Categories
                412
                Biological Sciences
                Developmental Biology

                chicken embryo,gonadal development,testis differentiation,ovary differentiation,sex determination

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