Identification of Novel Markers of Mouse Fetal Ovary Development

被引:38
作者
Chen, Huijun [1 ]
Palmer, James S. [1 ]
Thiagarajan, Rathi D. [1 ]
Dinger, Marcel E. [1 ]
Lesieur, Emmanuelle [1 ]
Chiu, Hansheng [1 ]
Schulz, Alexandra [1 ]
Spiller, Cassy [1 ]
Grimmond, Sean M. [1 ]
Little, Melissa H. [1 ]
Koopman, Peter [1 ]
Wilhelm, Dagmar [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Div Mol Genet & Dev, Brisbane, Qld, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
LONG NONCODING RNAS; MAMMALIAN SEX DETERMINATION; TRANSCRIPTION FACTOR FOXL2; X-CHROMOSOME INACTIVATION; DOUBLESEX-RELATED GENES; GERM-CELLS; TESTIS DEVELOPMENT; BETA-CATENIN; DETERMINATION REVEALS; EMBRYONIC GONAD;
D O I
10.1371/journal.pone.0041683
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In contrast to the developing testis, molecular pathways driving fetal ovarian development have been difficult to characterise. To date no single master regulator of ovarian development has been identified that would be considered the female equivalent of Sry. Using a genomic approach we identified a number of novel protein-coding as well as non-coding genes that were detectable at higher levels in the ovary compared to testis during early mouse gonad development. We were able to cluster these ovarian genes into different temporal expression categories. Of note, Lrrc34 and AK015184 were detected in XX but not XY germ cells before the onset of sex-specific germ cell differentiation marked by entry into meiosis in an ovary and mitotic arrest in a testis. We also defined distinct spatial expression domains of somatic cell genes in the developing ovary. Our data expands the set of markers of early mouse ovary differentiation and identifies a classification of early ovarian genes, thus providing additional avenues with which to dissect this process.
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页数:15
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