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Cloning and expression analysis of androgen receptor gene in chicken embryogenesis

机译:鸡胚胎发生过程中雄激素受体基因的克隆与表达分析

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We cloned a full-length androgen receptor (AR) cDNA from chicken (Gallus gallus) gonads. The cDNA sequence has an open reading frame of 2109 bp encoding 703 amino acids. The chicken AR (cAR) shares high homology with ARs from other species in its amino acid sequences, in particular DNA binding domain (DBD) and ligand binding domain (LBD). RT-PCR analysis revealed that cAR mRNA is expressed in several embryonic tissues of both sexes, and relatively higher expression was observed in left ovary compared with testis. The immunoreactive signal of A R was co-localized within the ovarian cell nucleus, while such nuclear localization was not detected in those of testis. To get insight on the possible role of androgen-AR signaling during gonadal development, non-steroidal AR antagonist, flutamide, was administrated in ovo. The treatment induced the disorganization of sex cords in ovarian cortex at day 12 of incubation. The effect was restored by testosterone co-treatment, implying the possibility that AR mediated signaling may be involved in ovarian morphogenesis. Furthermore, co-treatment of flutamide with estradiol-17 beta (E2) also restored the phenotype, suggesting androgen-AR signaling might activate aromatase expression that is necessary for estrogen synthesis. These findings suggest androgen-AR signaling might contribute to chicken embryonic ovarian development. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
机译:我们从鸡(性鸡)性腺中克隆了全长雄激素受体(AR)cDNA。 cDNA序列的2109 bp开放阅读框编码703个氨基酸。鸡AR(cAR)在氨基酸序列上与其他物种的AR具有高度同源性,尤其是DNA结合域(DBD)和配体结合域(LBD)。 RT-PCR分析显示,cAR mRNA在男女的几个胚胎组织中表达,与睾丸相比,在左卵巢中观察到相对较高的表达。 A R的免疫反应信号共定位在卵巢细胞核内,而在睾丸中未检测到这种核定位。为了深入了解雄激素-AR信号在性腺发育过程中的可能作用,在卵内施用了非甾体类AR拮抗剂氟他胺。在孵育的第12天,该处理诱导了卵巢皮质中性索的混乱。该作用通过睾丸激素的共同治疗得以恢复,这暗示了AR介导的信号传导可能参与了卵巢的形态发生。此外,氟他胺与雌二醇-17β(E2)的共处理也恢复了表型,表明雄激素-AR信号传导可能会激活雌激素合成所必需的芳香化酶表达。这些发现表明雄激素AR信号可能有助于鸡胚胎卵巢发育。 (c)2006年欧洲生物化学学会联合会。由Elsevier B.V.发布。保留所有权利。

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