...
首页> 外文期刊>The Journal of Reproduction and Development >Prominent expression of spinocerebellar ataxia type-1 (SCA1) gene encoding ataxin-1 in LH-producing cells, LbetaT2
【24h】

Prominent expression of spinocerebellar ataxia type-1 (SCA1) gene encoding ataxin-1 in LH-producing cells, LbetaT2

机译:在产LH的细胞LbetaT2中,编码小分子紫杉素-1的脊髓小脑共济失调1型(SCA1)基因的突出表达

获取原文
获取原文并翻译 | 示例

摘要

The LH-producing cell line, LbetaT2, and non LH-producing cell line, alphaT3-1 cells, established from a pituitary tumor, were employed for cDNA subtraction cloning to identify genes with expression unique to LH producing cells. Several cDNAs that code for known as well as for many unidentified clones were discovered. Most clones were the spinocerebellar ataxia type-1 (SCA1) gene encoding ataxin-1, the abnormality of which causes neurodegeneration and loss of cerebellar Purkinje cells. We examined whether the expression of SCA1 gene in LbetaT2 cells is related to hormone production. We also compared the expression of SCA1 with that in various other pituitary tumor derived cell lines, and confirmed the prominent expression of SCA1 in LbetaT2 cells. The effect of gonadal factor(s) for SCA1 gene expression was examined. The expression level in female rats was low and did not change during the estrus cycle, but increased significantly after ovariectomy and did not return to the normal level under low and high doses of estrogen. In the male pituitary SCA1 gene expression increased markedly after castration and was not decreased by estrogen or testosterone. The Ontogeny of SCA1 gene expression was investigated in porcine fetal and postnatal pituitaries and revealed biphasic and sexually dimorphic expression. Transient expression of SCA1 gene was observed at fetal day 50 and 65 in males and day 40 in females, followed by a decline and increased expression before birth in both genders. Thus the expression of SCA1 gene is prominent in LH-producing cells and is not under direct control of gonadal factor(s) in both genders. In addition to the variable expression of SCA1 gene during the fetus period, the present results provide a novel aspect to the understanding of Boucher-Neuhauser syndrome (Ataxia Hypogonadism Choroidal Dystrophy).
机译:从垂体瘤建立的LH产生细胞系LbetaT2和非LH产生细胞系alphaT3-1细胞用于cDNA减法克隆,以鉴定具有LH产生细胞独特表达的基因。发现了几种编码已知以及许多未鉴定克隆的cDNA。大多数克隆是编码小分子紫杉素-1的脊髓小脑共济失调1型(SCA1)基因,其异常导致神经变性和小脑浦肯野细胞的丢失。我们检查了LbetaT2细胞中SCA1基因的表达是否与激素产生有关。我们还比较了SCA1的表达与各种其他垂体肿瘤来源的细胞系中的表达,并证实了SCA1在LbetaT2细胞中的突出表达。检查了性腺因子对SCA1基因表达的影响。雌性大鼠中的表达水平低,在发情周期中没有变化,但在卵巢切除后明显增加,在低剂量和高剂量雌激素下均未恢复到正常水平。在雄性垂体中,SCA1基因的表达在去势后显着增加,而未被雌激素或睾丸激素降低。在猪胎儿和产后垂体中研究了SCA1基因的表达的个体发生,并揭示了双相和性二态表达。在胎儿的第50和65天观察到SCA1基因的瞬时表达,在女性的第40天观察到SCA1基因的瞬时表达,随后在男女出生前表达下降并增加。因此,SCA1基因的表达在产LH的细胞中很明显,并且在两个性别中均不受性腺因子的直接控制。除了在胎儿期SCA1基因的可变表达外,本研究结果为了解Boucher-Neuhauser综合征(共济失调性性腺减退性脉络膜营养不良症)提供了一个新的方面。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号