首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Vitamin D and adaptation to dietary calcium and phosphate deficiencies increase intestinal plasma membrane calcium pump gene expression.
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Vitamin D and adaptation to dietary calcium and phosphate deficiencies increase intestinal plasma membrane calcium pump gene expression.

机译:维生素D和对饮食中钙和磷酸盐缺乏症的适应能力增加了肠质膜钙泵基因的表达。

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摘要

The effect of vitamin D and other variables on the synthesis of the chicken intestinal plasma membrane calcium pump (PMCA) mRNA was assessed. The DNA probe for Northern analysis was obtained by reverse transcription and PCR with intestinal poly(A)+ RNA, using two 20-mer oligonucleotide primers homologous to the 3' coding region of the human teratoma PMCA. An EcoRI restriction fragment of the PCR product was cloned into the pBluescript II KS(-) phagemid vector, and the chimeric plasmid was used to transform Escherichia coli. The amino acid sequence deduced from the nucleotide DNA sequence of the PCR product and the cloned DNA were 96% homologous with the teratoma sequence. Northern blots of intestinal poly(A)+ RNA with 32P-labeled DNA showed the presence of three major species of chicken PMCA mRNAs at about 6.6, 5.4, and 4.5 kb. Northern analysis with the chicken PMCA DNA indicated that repletion of vitamin D-deficient chickens with vitamin D increased PMCA mRNAs in the duodenum, jejunum, ileum, and colon. After injection of 1,25-dihydroxyvitamin D3 intravenously into vitamin D-deficient chickens, duodenal PMCA mRNA tended to increase by 2 hr, reached a maximum at about 16 hr, and returned to baseline levels at 48 hr. Adaptation of chickens to either a calcium- or phosphorus-deficient diet resulted in a 2- to 3-fold increase in duodenal PMCA mRNA. These results indicate that vitamin D and specific variables that affect calcium absorption through the vitamin D-endocrine system increase intestinal PMCA gene expression.
机译:评估了维生素D和其他变量对鸡肠质膜钙泵(PMCA)mRNA合成的影响。使用两个与人畸胎瘤PMCA的3'编码区同源的20-mer寡核苷酸引物,通过反转录和PCR肠多聚(A)+ RNA获得用于Northern分析的DNA探针。将PCR产物的EcoRI限制性酶切片段克隆到pBluescript II KS(-)噬菌粒载体中,并将​​该嵌合质粒用于转化大肠杆菌。从PCR产物的核苷酸DNA序列推导的氨基酸序列和克隆的DNA与畸胎瘤序列96%同源。带有32P标记的DNA的肠道poly(A)+ RNA的Northern印迹表明,存在三种主要的鸡PMCA mRNA,分别约为6.6、5.4和4.5 kb。用鸡PMCA DNA进行的Northern分析表明,维生素D缺乏的鸡补充维生素D会增加十二指肠,空肠,回肠和结肠中PMCA mRNA的表达。在向缺乏维生素D的鸡中静脉注射1,25-二羟基维生素D3后,十二指肠PMCA mRNA倾向于增加2小时,在大约16小时达到最大值,并在48小时回到基线水平。使鸡适应缺钙或缺磷饮食会导致十二指肠PMCA mRNA增加2-3倍。这些结果表明,维生素D和影响通过维生素D-内分泌系统吸收钙的特定变量会增加肠道PMCA基因的表达。

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