Division of Endocrinology, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Mol Cell Endocrinol. 2013 Jan 30;365(2):241-8. doi: 10.1016/j.mce.2012.10.025. Epub 2012 Nov 5.
Genome-wide association studies recently identified 32 loci that associate with the age at menarche (AAM) in humans. Because the locus most robustly associated with AAM is in/near LIN28B, the goal of this study was to investigate how the Lin28 pathway might modulate pubertal timing by examining expression of Lin28b, and its homologue, Lin28a, across the pubertal transition in female mice. Quantitative reverse-transcriptase PCR data indicate that, prior to the onset of puberty, expression of both Lin28b and Lin28a decreases in the ovary, while expression of only Lin28a decreases in the hypothalamus; the expression of Lin28a increases after the onset of puberty in the pituitary. Immunohistochemistry in ovarian tissue verified that Lin28a protein levels decreased in parallel with gene expression. Although these data do not demonstrate cause and effect, they do suggest that decreased expression of Lin28a/Lin28b may facilitate the transition into puberty, consistent with previous data showing that overexpression of Lin28a in transgenic mice leads to delayed puberty. In addition, although Lin28b and/or Lin28a expression significantly decreased prior to puberty, neither Let-7a nor Let-7g miRNA levels changed significantly, raising the possibility that some effects of Lin28b and Lin28a within the hypothalamic-pituitary-gonadal (HPG) axis may be Let-7 miRNA independent. Subsequent studies, such as tissue and age specific modulation of Lin28b and Lin28a expression, could determine whether the expression patterns observed are responsible for modulating the onset of puberty and delineate further the role of this pathway in the HPG axis.
全基因组关联研究最近确定了 32 个与人类初潮年龄 (AAM) 相关的位点。由于与 AAM 最密切相关的位点位于 LIN28B 内/附近,因此本研究的目的是通过检查 Lin28b 和其同源物 Lin28a 在雌性小鼠青春期过渡过程中的表达,来研究 Lin28 通路如何调节青春期时间。定量逆转录酶 PCR 数据表明,在青春期开始之前,Lin28b 和 Lin28a 的表达在卵巢中均降低,而只有 Lin28a 的表达在下丘脑降低;Lin28a 的表达在青春期开始后在垂体中增加。卵巢组织中的免疫组织化学验证了 Lin28a 蛋白水平与基因表达平行下降。尽管这些数据不能证明因果关系,但它们确实表明 Lin28a/Lin28b 的表达降低可能有助于进入青春期,这与先前的数据一致,即转基因小鼠中 Lin28a 的过表达导致青春期延迟。此外,尽管 Lin28b 和/或 Lin28a 的表达在青春期前显著降低,但 Let-7a 或 Let-7g miRNA 水平没有显著变化,这表明 Lin28b 和 Lin28a 在下丘脑-垂体-性腺 (HPG) 轴中的某些作用可能与 Let-7 miRNA 无关。随后的研究,如组织和年龄特异性调节 Lin28b 和 Lin28a 的表达,可能确定观察到的表达模式是否负责调节青春期的开始,并进一步阐明该途径在 HPG 轴中的作用。