Sexual cell-fate reprogramming in the ovary by DMRT1

Robin E. Lindeman, Micah D. Gearhart, Anna Minkina, Anthony D. Krentz, Vivian J. Bardwell, David Zarkower

Research output: Contribution to journalArticlepeer-review

68 Scopus citations

Abstract

Transcription factors related to the insect sex-determination gene doublesex (DMRT proteins) control sex determination and/or sexual differentiation in diverse metazoans and are implicated in transitions between sex-determining mechanisms during vertebrate evolution [1]. In mice, Dmrt1 is required for male gonadal differentiation in somatic cells and germ cells [2-4]. DMRT1 also maintains male gonadal sex: its loss, even in adults, can trigger sexual cell-fate reprogramming in which male Sertoli cells transdifferentiate into their female equivalents - granulosa cells - and testicular tissue reorganizes to a more ovarian morphology [5]. Here we use a conditional Dmrt1 transgene to show that Dmrt1 is not only necessary but also sufficient to specify male cell identity in the mouse gonad. DMRT1 expression in the ovary silenced the female sex-maintenance gene Foxl2 and reprogrammed juvenile and adult granulosa cells into Sertoli-like cells, triggering formation of structures resembling male seminiferous tubules. DMRT1 can silence Foxl2 even in the absence of the testis-determining genes Sox8 and Sox9. mRNA profiling found that DMRT1 activates many testicular genes and downregulates ovarian genes and single-cell RNA sequencing in transdifferentiating cells identified dynamically expressed candidate mediators of this process. Strongly upregulated genes were highly enriched on chromosome X, consistent with sexually antagonistic functions. This study provides an in vivo example of single-gene reprogramming of cell sexual identity. Our findings suggest a reconsideration of mechanisms involved in human disorders of sex development (DSDs) and empirically support evolutionary models in which loss or gain of Dmrt1 function promotes establishment of new vertebrate sex-determination systems.

Original languageEnglish (US)
Pages (from-to)764-771
Number of pages8
JournalCurrent Biology
Volume25
Issue number6
DOIs
StatePublished - Mar 16 2015

Bibliographical note

Funding Information:
We thank M. Wegner for SOX8 antibodies, F. Poulat for SOX9 antibodies, R. Behringer, E. Brown, E. Casanova, M. Lewandoski, K. Parker, G. Scherer, M. Treier, and M. Wegner for mice, R. Behringer for advice, C. Corcoran for technical assistance, and M. Murphy for helpful discussions. This work was supported by the NIH (5 R01 GM59152 and 1 F32 GM106484), Minnesota Medical Foundation, University of Minnesota Medical School and College of Biological Sciences, and University of Minnesota Genomics Center.

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