Laz Ekaterina V, Holloway Minita G, Chen Chong-Sheng, Waxman David J
Department of Biology, Boston University, 5 Cummington Street, Boston, Massachusetts 02215, USA.
Endocrinology. 2007 Jul;148(7):3327-37. doi: 10.1210/en.2006-1192. Epub 2007 Apr 5.
Plasma GH profiles regulate the sexually dimorphic expression of cytochromes P450 and many other genes in rat and mouse liver; however, the proximal transcriptional regulators of these genes are unknown. Presently, we characterize three liver transcription factors that are expressed in adult female rat and mouse liver at levels up to 16-fold [thymus high-mobility group box protein (Tox)], 73-fold [tripartite motif-containing 24 (Trim24)/transcription initiation factor-1alpha (TIF1alpha)], and 125-fold [cut-like 2 (Cutl2)/cut homeobox 2 (Cux2)] higher than in adult males, depending on the strain and species, with Tox expression only detected in mice. In rats, these sex differences first emerged at puberty, when the high prepubertal expression of Cutl2 and Trim24 was extinguished in males but was further increased in females. Rat hepatic expression of Cutl2 and Trim24 was abolished by hypophysectomy and, in the case of Cutl2, was restored to near-female levels by continuous GH replacement. Cutl2 and Trim24 were increased to female-like levels in livers of intact male rats and mice treated with GH continuously (female GH pattern), whereas Tox expression reached only about 40% of adult female levels. Expression of all three genes was also elevated to normal female levels or higher in male mice whose plasma GH profile was feminized secondary to somatostatin gene disruption. Cutl2 and Trim24 both responded to GH infusion in mice within 10-24 h and Tox within 4 d, as compared with at least 4-7 d required for the induced expression of several continuous GH-regulated cytochromes P450 and other female-specific hepatic genes. Cutl2, Trim24, and Tox were substantially up-regulated in livers of male mice deficient in either of two transcription factors implicated in GH regulation of liver sex specificity, namely, signal transducer and activator of transcription 5b (STAT5b) and hepatocyte nuclear factor 4alpha (HNF4alpha), with sex-specific expression being substantially reduced or lost in mice deficient in either nuclear factor. Cutl2 and Trim24 both display transcriptional repressor activity and could thus contribute to the loss of GH-regulated, male-specific liver gene expression seen in male mice deficient in STAT5b or HNF4alpha. Binding sites for Cutl1, whose DNA-binding specificity is close to that of Cutl2, were statistically overrepresented in STAT5b-dependent male-specific mouse genes, lending support to this hypothesis.
血浆生长激素(GH)谱调节大鼠和小鼠肝脏中细胞色素P450及许多其他基因的性别二态性表达;然而,这些基因的近端转录调节因子尚不清楚。目前,我们鉴定了三种肝脏转录因子,它们在成年雌性大鼠和小鼠肝脏中的表达水平比成年雄性高16倍[胸腺高迁移率族框蛋白(Tox)]、73倍[含三重基序的24(Trim24)/转录起始因子-1α(TIF1α)]和125倍[类切割蛋白2(Cutl2)/切割同源框2(Cux2)],具体倍数取决于品系和物种,且Tox表达仅在小鼠中检测到。在大鼠中,这些性别差异在青春期首次出现,此时雄性中Cutl2和Trim24青春期前的高表达消失,而雌性中则进一步增加。垂体切除可消除大鼠肝脏中Cutl2和Trim24的表达,对于Cutl2而言,持续给予生长激素替代可使其恢复至接近雌性的水平。持续给予生长激素(雌性生长激素模式)处理的完整雄性大鼠和小鼠肝脏中,Cutl2和Trim24增加至类似雌性的水平,而Tox表达仅达到成年雌性水平的约40%。在因生长抑素基因破坏导致血浆生长激素谱女性化的雄性小鼠中,这三种基因的表达也升高至正常雌性水平或更高。与几种持续生长激素调节的细胞色素P450及其他雌性特异性肝脏基因诱导表达所需的至少4 - 7天相比,Cutl2和Trim24在小鼠中对生长激素输注在10 - 24小时内有反应,Tox在4天内有反应。在涉及肝脏性别特异性生长激素调节的两种转录因子之一缺陷的雄性小鼠肝脏中,Cutl2、Trim24和Tox显著上调,即信号转导子和转录激活子5b(STAT5b)和肝细胞核因子4α(HNF4α),在任一核因子缺陷的小鼠中,性别特异性表达显著降低或丧失。Cutl2和Trim24均显示转录抑制活性,因此可能导致在STAT5b或HNF4α缺陷的雄性小鼠中出现生长激素调节的雄性特异性肝脏基因表达丧失。Cutl1的结合位点,其DNA结合特异性与Cutl2接近,在STAT5b依赖性雄性特异性小鼠基因中在统计学上过度表达,支持了这一假说。