首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >MICE DEFICIENT IN THE ORPHAN RECEPTOR STEROIDOGENIC FACTOR I LACK ADRENAL GLANDS AND GONADS BUT EXPRESS P450 SIDE-CHAIN-CLEAVAGE ENZYME IN THE PLACENTA AND HAVE NORMAL EMBRYONIC SERUM LEVELS OF CORTICOSTEROIDS
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MICE DEFICIENT IN THE ORPHAN RECEPTOR STEROIDOGENIC FACTOR I LACK ADRENAL GLANDS AND GONADS BUT EXPRESS P450 SIDE-CHAIN-CLEAVAGE ENZYME IN THE PLACENTA AND HAVE NORMAL EMBRYONIC SERUM LEVELS OF CORTICOSTEROIDS

机译:缺乏ORPHAN受体的骨生成因子的小鼠,我缺乏肾上腺和性腺,但在胎盘中表达了P450侧链裂解酶,并具有正常的胚轴胚乳血清水平

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The orphan nuclear receptor steroidogenic factor 1 (SF-1) is expressed in the adrenal cortex and gonads and regulates the expression of several P450 steroid hydroxylases in vitro. We examined the role of SF-1 in the adrenal glands and gonads in vivo by a targeted disruption of the mouse SF-1 gene. All SF-1-deficient mice died shortly after delivery. Their adrenal glands and gonads were absent, and persistent Mullerian structures were found in all genotypic males. While serum levels of corticosterone in SF-1-deficient mice were diminished, levels of adrenocorticotropic hormone (ACTH) were elevated, consistent with intact pituitary corticotrophs. Intrauterine survival of SF-1 deficient mice appeared normal, and they had normal serum level of corticosterone and ACTK, probably reflecting transplacental passage of maternal steroids. We tested whether SF-1 is required for P450 side-chain-cleavage enzyme (P450scc) expression in the placenta, which expresses both SF-1 and P450scc, and found that in contrast to its strong activation of the P450scc gene promoter in vitro, the absence of SF-1 had no effect on P450scc mRNA levels in vivo. Although the region targeted by our disruption is shared by SF-1 and by embryonal long terminal repeat-binding protein (ELF), a hypothesized alternatively spliced product, we believe that the observed phenotype reflects absent SF-1 alone, as PCR analysis failed to detect ELF transcripts in any mouse tissue, and sequences corresponding to ELF are not conserved across species. These results confirm that SF-1 is an important regulator of adrenal and gonadal development, but its regulation of steroid hydroxylase expression in vivo remains to be established. [References: 32]
机译:孤儿核受体类固醇生成因子1(SF-1)在肾上腺皮质和性腺中表达,并在体外调节几种P450类固醇羟化酶的表达。我们通过有针对性地破坏小鼠SF-1基因,检查了SF-1在体内肾上腺和性腺中的作用。所有SF-1缺陷小鼠在分娩后不久死亡。他们的肾上腺和性腺不存在,并且在所有基因型男性中都发现了持久的穆勒结构。虽然SF-1缺陷小鼠的血清皮质酮水平降低,但促肾上腺皮质激素(ACTH)水平升高,与完整的垂体皮质激素一致。 SF-1缺陷型小鼠的宫内存活似乎正常,并且其皮质酮和ACTK的血清水平正常,这可能反映了母体类固醇经胎盘传递。我们测试了SF-1是胎盘中P450侧链切割酶(P450scc)表达所必需的,它同时表达SF-1和P450scc,并发现与在体外强烈激活P450scc基因启动子相反, SF-1的缺失对体内P450scc mRNA水平没有影响。尽管我们破坏的目标区域由SF-1和胚胎长末端重复结合蛋白(ELF)(一种假定的可变剪接产物)共享,但我们认为观察到的表型仅反映了SF-1的缺失,因为PCR分析无法检测任何小鼠组织中的ELF转录物,并且对应于ELF的序列在物种间并不保守。这些结果证实SF-1是肾上腺和性腺发育的重要调节剂,但其体内甾体羟化酶表达的调节仍有待建立。 [参考:32]

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