Tyson-Capper A J, Shiells E A, Robson S C
The Medical School, Institute of Cellular Medicine, Newcastle University, 3rd Floor, William Leech Building, Newcastle upon Tyne, UK.
J Mol Endocrinol. 2009 Jul;43(1):29-41. doi: 10.1677/JME-09-0001. Epub 2009 Apr 1.
The precise molecular mechanisms controlling progesterone receptor (PR)-mediated gene regulation within the human myometrium in pregnancy and in labour remain poorly defined. PR recruit different nuclear co-activators/co-repressors to mediate receptor-specific transcription regulation and expression of PR, and these co-factors may alter within the myometrium during pregnancy and labour. The aims of this study were to test the hypotheses that i) the human splicing and transcription factor, polypyrimidine tract binding protein-associated splicing factor (PSF), is spatially and temporally regulated in the myometrium during pregnancy and labour; ii) PSF influences the expression of myometrial PR and iii) the action of PR in regulating specific hormone response target genes in the human myometrium may involve PSF. Immunoblotting indicated that PSF expression is significantly up-regulated within the human myometrium as pregnancy progresses, in particular within the upper uterine region, and levels remain elevated in labour. Co-immunoprecipitations and DNA-binding assays show that PSF directly interacts with nuclear PR and glucocorticoid receptor (GR) and specific co-regulatory proteins, all of which have defined roles as co-activators or co-repressors in gene regulation. Over-expression and inhibition of PSF by transient transfection and RNAi respectively alters expression of myometrial PR and GR and may influence expression of two PR/GR-target genes, cyclooxygenase-2 and histone deacetylase-2. These findings are suggestive of a role for myometrial PSF as a nuclear co-regulator in the regulation of specific hormone receptor genes and their target hormone response genes.
在妊娠和分娩期间,控制人子宫肌层中孕激素受体(PR)介导的基因调控的精确分子机制仍不清楚。PR招募不同的核共激活因子/共抑制因子来介导受体特异性转录调控和PR的表达,并且这些辅助因子在妊娠和分娩期间可能在子宫肌层内发生变化。本研究的目的是检验以下假设:i)人剪接和转录因子,多嘧啶序列结合蛋白相关剪接因子(PSF),在妊娠和分娩期间在子宫肌层中受到时空调控;ii)PSF影响子宫肌层PR的表达;iii)PR在调节人子宫肌层中特定激素反应靶基因的作用可能涉及PSF。免疫印迹表明,随着妊娠进展,PSF在人子宫肌层内显著上调,尤其是在子宫上部区域,并且在分娩时水平仍然升高。免疫共沉淀和DNA结合试验表明,PSF直接与核PR和糖皮质激素受体(GR)以及特定的共调节蛋白相互作用,所有这些蛋白在基因调控中都具有作为共激活因子或共抑制因子的明确作用。分别通过瞬时转染和RNAi过表达和抑制PSF会改变子宫肌层PR和GR的表达,并可能影响两个PR/GR靶基因环氧合酶-2和组蛋白去乙酰化酶-2的表达。这些发现提示子宫肌层PSF作为核共调节因子在调节特定激素受体基因及其靶激素反应基因中发挥作用。