Foxl2 is required for commitment to ovary differentiation
Genetic control of female sex differentiation from a bipotential gonad in mammals is poorly understood. We find that mouse XX gonads lacking the forkhead transcription factor Foxl2 form meiotic prophase oocytes, but then activate the genetic program for somatic testis determination. Pivotal Foxl2 ac...
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| Published in: | Human molecular genetics Vol. 14; no. 14; p. 2053 |
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| Main Authors: | , , , , , , , |
| Format: | Journal Article |
| Language: | English |
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15.07.2005
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| ISSN: | 0964-6906 |
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| Abstract | Genetic control of female sex differentiation from a bipotential gonad in mammals is poorly understood. We find that mouse XX gonads lacking the forkhead transcription factor Foxl2 form meiotic prophase oocytes, but then activate the genetic program for somatic testis determination. Pivotal Foxl2 action thus represses the male gene pathway at several stages of female gonadal differentiation. This suggests the possible continued involvement of sex-determining genes in maintaining ovarian function throughout female reproductive life. |
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| AbstractList | Genetic control of female sex differentiation from a bipotential gonad in mammals is poorly understood. We find that mouse XX gonads lacking the forkhead transcription factor Foxl2 form meiotic prophase oocytes, but then activate the genetic program for somatic testis determination. Pivotal Foxl2 action thus represses the male gene pathway at several stages of female gonadal differentiation. This suggests the possible continued involvement of sex-determining genes in maintaining ovarian function throughout female reproductive life. Genetic control of female sex differentiation from a bipotential gonad in mammals is poorly understood. We find that mouse XX gonads lacking the forkhead transcription factor Foxl2 form meiotic prophase oocytes, but then activate the genetic program for somatic testis determination. Pivotal Foxl2 action thus represses the male gene pathway at several stages of female gonadal differentiation. This suggests the possible continued involvement of sex-determining genes in maintaining ovarian function throughout female reproductive life.Genetic control of female sex differentiation from a bipotential gonad in mammals is poorly understood. We find that mouse XX gonads lacking the forkhead transcription factor Foxl2 form meiotic prophase oocytes, but then activate the genetic program for somatic testis determination. Pivotal Foxl2 action thus represses the male gene pathway at several stages of female gonadal differentiation. This suggests the possible continued involvement of sex-determining genes in maintaining ovarian function throughout female reproductive life. |
| Author | Uda, Manuela Pilia, Giuseppe Omari, Shakib Garcia-Ortiz, J Elias Crisponi, Laura Schlessinger, David Forabosco, Antonino Ottolenghi, Chris |
| Author_xml | – sequence: 1 givenname: Chris surname: Ottolenghi fullname: Ottolenghi, Chris organization: Laboratory of Genetics, National Institute on Aging, Baltimore, MD 21224, USA – sequence: 2 givenname: Shakib surname: Omari fullname: Omari, Shakib – sequence: 3 givenname: J Elias surname: Garcia-Ortiz fullname: Garcia-Ortiz, J Elias – sequence: 4 givenname: Manuela surname: Uda fullname: Uda, Manuela – sequence: 5 givenname: Laura surname: Crisponi fullname: Crisponi, Laura – sequence: 6 givenname: Antonino surname: Forabosco fullname: Forabosco, Antonino – sequence: 7 givenname: Giuseppe surname: Pilia fullname: Pilia, Giuseppe – sequence: 8 givenname: David surname: Schlessinger fullname: Schlessinger, David |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/15944199$$D View this record in MEDLINE/PubMed |
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| SubjectTerms | Animals Female Forkhead Box Protein L2 Forkhead Transcription Factors - genetics Immunohistochemistry Mice Microscopy, Electron Ovary - embryology Ovary - physiology Ovary - ultrastructure Sex Differentiation - genetics |
| Title | Foxl2 is required for commitment to ovary differentiation |
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