Cai Q, Chandler J S, Wasserman R H, Kumar R, Penniston J T
Department of Physiology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.
Proc Natl Acad Sci U S A. 1993 Feb 15;90(4):1345-9. doi: 10.1073/pnas.90.4.1345.
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.
评估了维生素D和其他变量对鸡肠道质膜钙泵(PMCA)mRNA合成的影响。用于Northern分析的DNA探针是通过逆转录和PCR获得的,使用与人畸胎瘤PMCA的3'编码区同源的两个20聚体寡核苷酸引物,以肠道poly(A)+RNA为模板。PCR产物的EcoRI限制性片段被克隆到pBluescript II KS(-)噬菌粒载体中,并且该嵌合质粒用于转化大肠杆菌。从PCR产物和克隆DNA的核苷酸DNA序列推导的氨基酸序列与畸胎瘤序列的同源性为96%。用32P标记的DNA对肠道poly(A)+RNA进行Northern印迹分析,结果显示存在三种主要的鸡PMCA mRNA,大小约为6.6、5.4和4.5 kb。用鸡PMCA DNA进行Northern分析表明,用维生素D补充维生素D缺乏的鸡,十二指肠、空肠、回肠和结肠中的PMCA mRNA增加。向维生素D缺乏的鸡静脉注射1,25-二羟基维生素D3后,十二指肠PMCA mRNA在2小时时趋于增加,在约16小时时达到最大值,并在48小时时恢复到基线水平。鸡适应缺钙或缺磷饮食会导致十二指肠PMCA mRNA增加2至3倍。这些结果表明,维生素D以及通过维生素D内分泌系统影响钙吸收的特定变量会增加肠道PMCA基因的表达。