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人甲状旁腺激素基因的组织和基因特异性低甲基化:与甲状旁腺中甲状旁腺激素基因表达的关联

Tissue and gene specific hypomethylation of the human parathyroid hormone gene: association with parathyroid hormone gene expression in parathyroid glands.

作者信息

Levine M A, Morrow P P, Kronenberg H M, Phillips J A

出版信息

Endocrinology. 1986 Oct;119(4):1618-24. doi: 10.1210/endo-119-4-1618.

Abstract

An association between decreased cytosine methylation at specific sites adjacent to or within eukaryotic genes and increased gene expression has been described. To determine if tissues secreting PTH show hypomethylation within the vicinity of the PTH gene, we compared the degree of cytosine methylation in DNA from parathyroid glands and control tissues (leukocytes, anterior pituitary, posterior pituitary, and placenta). We digested DNA with HpaII (which cleaves only unmethylated CCGG sequences) and MspI [which cleaves CCGG and C 5-methyl cytosine GG], hybridized the DNA fragments to a PTH complementary DNA probe, and scanned autoradiograms of Southern blots. After MspI digestion all tissues yielded equivalent amounts of a single hybridizing fragment of 6.7 kilobases. The degree of hypomethylation at sites within and flanking the PTH gene was determined as the ratio of the amount of hybridizing fragments obtained by methylation-sensitive digestion (HpaII) relative to methylation-insensitive digestion (MspI). DNA from all parathyroid glands showed significantly greater hypomethylation of the PTH gene than did DNA from control tissues that did not express the PTH gene. Despite variability in the levels of secretory activity of the different parathyroid glands, we found no significant differences in the degree of hypomethylation of the PTH gene. In contrast to the PTH gene studies, hypomethylation was not seen using GH probe on the same blots. Our findings thus suggest that tissue and gene specific hypomethylation of the PTH gene is associated with expression of the gene.

摘要

真核基因相邻或内部特定位点的胞嘧啶甲基化降低与基因表达增加之间的关联已有描述。为了确定分泌甲状旁腺激素(PTH)的组织中PTH基因附近是否存在低甲基化,我们比较了甲状旁腺和对照组织(白细胞、垂体前叶、垂体后叶和胎盘)DNA中的胞嘧啶甲基化程度。我们用HpaII(仅切割未甲基化的CCGG序列)和MspI [切割CCGG和C5 - 甲基胞嘧啶GG]消化DNA,使DNA片段与PTH互补DNA探针杂交,并扫描Southern印迹的放射自显影片。MspI消化后,所有组织均产生等量的单一6.7千碱基杂交片段。PTH基因内部和侧翼位点的低甲基化程度通过甲基化敏感消化(HpaII)获得的杂交片段量与甲基化不敏感消化(MspI)获得的杂交片段量之比来确定。所有甲状旁腺的DNA显示出PTH基因的低甲基化程度明显高于不表达PTH基因的对照组织的DNA。尽管不同甲状旁腺的分泌活性水平存在差异,但我们发现PTH基因的低甲基化程度没有显著差异。与PTH基因研究相反,在同一印迹上使用生长激素(GH)探针未观察到低甲基化。因此,我们的研究结果表明,PTH基因的组织和基因特异性低甲基化与该基因的表达相关。

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