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鉴定小鼠胎儿卵巢发育的新型标志物。

Identification of novel markers of mouse fetal ovary development.

机构信息

Division of Molecular Genetics and Development, Institute for Molecular Biosciences, The University of Queensland, Brisbane, Australia.

出版信息

PLoS One. 2012;7(7):e41683. doi: 10.1371/journal.pone.0041683. Epub 2012 Jul 26.

Abstract

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.

摘要

与发育中的睾丸相比,驱动胎儿卵巢发育的分子途径一直难以描述。迄今为止,尚未发现单一的卵巢发育主调控因子可以被认为是 Sry 的女性对应物。我们使用基因组方法鉴定了许多新的蛋白编码基因和非编码基因,这些基因在早期小鼠性腺发育过程中,在卵巢中的表达水平明显高于睾丸。我们能够将这些卵巢基因聚类为不同的时间表达类别。值得注意的是,在 XX 性生殖细胞进入减数分裂之前,即 XY 性生殖细胞进入性别特异性生殖细胞分化之前,LRRC34 和 AK015184 就已经在卵巢中被检测到,但在睾丸中没有被检测到。我们还在发育中的卵巢中定义了体细胞基因的不同空间表达区域。我们的数据扩展了早期小鼠卵巢分化的标记物集,并确定了早期卵巢基因的分类,从而为剖析这一过程提供了更多的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87c2/3406020/d251c243e6fa/pone.0041683.g001.jpg

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