About 1-3% of all women undergo precocious menopause, either never going through menarche or stopping menstruation by the mid-30's, rather than reaching the standard reproductive lifespan of about 50. A fraction of such instances of early-onset """"""""premature ovarian failure (POF)"""""""" is genetic. A single locus on chromosome 3 is implicated in several families and in several isolated individuals with translocations or deletions that interrupt the DNA in that region. In collaboration with the group of Dr. G. Pilia, we have isolated the gene, FOXL2, in which mutations cause POF, and are analyzing its function; it appears to function as a rheostat, determining the number of follicles by the level of its function. Currently, we have recovered the mouse orthologue, Foxl2, and are developing a mouse model for its insufficiency by constructing animals in which the gene is disrupted. A much larger group of translocations on the X chromosome, centering on a critical region of the long arm, have been associated with POF. We have now shown that based on the physical map we had constructed, there are at least 35 distinct X chromosome loci at which translocations can produce POF. We have begun further molecular analyses of the sequences spanning translocation breakpoints. Three have been analyzed in detail at the sequence level, and two of these fall outside of any gene, in regions of repetitive sequence elements. This increases the possibility that some X translocations act by interrupting chromosome dynamics during meiosis, whereas others may cause POF by the interruption of specific genes involved in follicle formation or stability. To help understand the failure of follicle formation and maintenance in POF, we have begun an auxiliary project to analyze normal ovarian development. We are using gene expression profiling on microarrays of 15K mouse cDNAs (the NIA array developed by the group of Dr. M. Ko (LG)) to assess the gene cohorts involved in ovary formation. We have thus far compared the profile of genes expressed in nascent ovary, from newborn mice in which ovarian follicles are just starting to be formed, with mature ovary, in which follicles are fully formed. Marker genes expressed in follicle cells only at birth, or in oocytes of nascent or in mature mice have been recovered for further functional studies. These will be analyzed along with genes whose function is sharply affected in hereditary POF, using the mouse model that is under construction with Foxl2 disrupted. In that model, the point of interruption of programmed, coordinated gene function will be assessed by determining the target genes under the control of Foxl2.
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| Ottolenghi, Chris; Pelosi, Emanuele; Tran, Joseph et al. (2007) Loss of Wnt4 and Foxl2 leads to female-to-male sex reversal extending to germ cells. Hum Mol Genet 16:2795-804 |
| Kouprina, Natalay; Noskov, Vladimir N; Pavlicek, Adam et al. (2007) Evolutionary diversification of SPANX-N sperm protein gene structure and expression. PLoS ONE 2:e359 |
| Ottolenghi, Chris; Colombino, Maria; Crisponi, Laura et al. (2007) Transcriptional control of ovarian development in somatic cells. Semin Reprod Med 25:252-63 |
| Ottolenghi, Chris; Uda, Manuela; Crisponi, Laura et al. (2007) Determination and stability of sex. Bioessays 29:15-25 |
| Bowl, Michael R; Nesbit, M Andrew; Harding, Brian et al. (2005) An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism. J Clin Invest 115:2822-31 |
| Herrera, Luisa; Ottolenghi, Chris; Garcia-Ortiz, J Elias et al. (2005) Mouse ovary developmental RNA and protein markers from gene expression profiling. Dev Biol 279:271-90 |
| Ottolenghi, Chris; Omari, Shakib; Garcia-Ortiz, J Elias et al. (2005) Foxl2 is required for commitment to ovary differentiation. Hum Mol Genet 14:2053-62 |
| (2005) The DNA sequence of the human X chromosome. Nature 434:325-37 |
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