Breast Cancer Functional Genomics Laboratory, Cancer Research UK Cambridge Research Institute and Department of Oncology, University of Cambridge, Li Ka Shing Centre, Cambridge, UK.
BMC Genomics. 2009 Nov 20;10:548. doi: 10.1186/1471-2164-10-548.
The differential expression pattern of microRNAs (miRNAs) during mammary gland development might provide insights into their role in regulating the homeostasis of the mammary epithelium. Our aim was to analyse these regulatory functions by deriving a comprehensive tissue-specific combined miRNA and mRNA expression profile of post-natal mouse mammary gland development.We measured the expression of 318 individual murine miRNAs by bead-based flow-cytometric profiling of whole mouse mammary glands throughout a 16-point developmental time course, including juvenile, puberty, mature virgin, gestation, lactation, and involution stages. In parallel whole-genome mRNA expression data were obtained.
One third (n = 102) of all murine miRNAs analysed were detected during mammary gland development. MicroRNAs were represented in seven temporally co-expressed clusters, which were enriched for both miRNAs belonging to the same family and breast cancer-associated miRNAs. Global miRNA and mRNA expression was significantly reduced during lactation and the early stages of involution after weaning. For most detected miRNA families we did not observe systematic changes in the expression of predicted targets. For miRNA families whose targets did show changes, we observed inverse patterns of miRNA and target expression. The data sets are made publicly available and the combined expression profiles represent an important community resource for mammary gland biology research.
MicroRNAs were expressed in likely co-regulated clusters during mammary gland development. Breast cancer-associated miRNAs were significantly enriched in these clusters. The mechanism and functional consequences of this miRNA co-regulation provide new avenues for research into mammary gland biology and generate candidates for functional validation.
乳腺发育过程中 microRNAs(miRNAs)的差异表达模式可能为其在调节乳腺上皮细胞稳态中的作用提供线索。我们的目的是通过对产后小鼠乳腺发育的综合组织特异性 miRNA 和 mRNA 表达谱进行分析来研究这些调节功能。
我们通过对整个小鼠乳腺在 16 个发育时间点(包括幼年期、青春期、成熟未孕期、妊娠期、哺乳期和退化期)的流式细胞术 bead-based 分析,测量了 318 个单个鼠 miRNA 的表达。同时获得了全基因组 mRNA 表达数据。
在乳腺发育过程中检测到分析的所有 miRNA 中的三分之一(n = 102)。miRNAs 分为七个时间上共表达的簇,这些簇富含同一家族的 miRNA 和乳腺癌相关 miRNA。在哺乳期和断奶后早期退化阶段,miRNA 和 mRNA 的整体表达显著降低。对于大多数检测到的 miRNA 家族,我们没有观察到预测靶标表达的系统变化。对于靶标确实发生变化的 miRNA 家族,我们观察到 miRNA 和靶标表达的相反模式。数据集是公开的,组合表达谱代表乳腺生物学研究的重要社区资源。
在乳腺发育过程中,miRNAs 以可能的共调控簇的形式表达。这些簇中显著富集了乳腺癌相关的 miRNAs。这种 miRNA 共调控的机制和功能后果为乳腺生物学的研究提供了新的途径,并为功能验证生成了候选物。