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Til 1——一种DNA甲基化程度极低的人淋巴母细胞系。

Til 1--a human lymphoblastoid cell line with minimal DNA methylation.

作者信息

Lindsay S, Adams R L, Monk M

机构信息

MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.

出版信息

Hum Genet. 1989 Feb;81(3):252-6. doi: 10.1007/BF00278999.

Abstract

Methylation has been shown to be correlated with several fundamental cellular processes, including changes in gene expression, alterations in chromatin structure and inactivation of the mammalian X chromosome. It is possible, therefore, that the methylation status of a particular sequence may reflect involvement in a number of processes. Given this potentially confused situation, it is clear that many studies would be facilitated if unmethylated or minimally methylated DNA from a mammalian source were available. A major use of such DNA would be in the construction of long-range physical maps. In many cases, long-range physical maps are a prerequisite for the eventual isolation of disease genes that have been localised to a particular chromosomal region by other means (e.g. genetic linkage studies). Many of the enzymes used in such long-range mapping experiments are methylation sensitive, which makes it difficult to determine how many sites for a particular enzyme are present in any DNA sequence. Here we report the finding of a minimally methylated DNA in the human lymphoblastoid cell line, Til 1. The methylation level of Til 1 DNA was analysed in several ways and compared with that in human lymphocytes, placental tissue and other lymphoblastoid cell lines. The results showed clear and reproducible differences in methylation among the cell types, both at a global level and in the vicinities of specific DNA sequences. Lymphocyte DNA had the highest level of methylation while placental DNA and cell line DNA had lower but similar levels. Til 1 had abnormally low levels of 5-methylcytosine when measured directly, and no detectable methylation at any of the restriction sites examined.

摘要

甲基化已被证明与多种基本细胞过程相关,包括基因表达的变化、染色质结构的改变以及哺乳动物X染色体的失活。因此,特定序列的甲基化状态可能反映其参与了多个过程。鉴于这种潜在的复杂情况,很明显,如果能获得来自哺乳动物的未甲基化或甲基化程度最低的DNA,将有助于开展许多研究。这种DNA的一个主要用途是构建长程物理图谱。在许多情况下,长程物理图谱是最终分离通过其他方法(如遗传连锁研究)定位到特定染色体区域的疾病基因的先决条件。此类长程图谱实验中使用的许多酶对甲基化敏感,这使得难以确定任何DNA序列中特定酶的位点数量。在此,我们报告在人淋巴母细胞系Til 1中发现了一种甲基化程度最低的DNA。我们用多种方法分析了Til 1 DNA的甲基化水平,并与人类淋巴细胞、胎盘组织和其他淋巴母细胞系的甲基化水平进行了比较。结果表明,在整体水平以及特定DNA序列附近,不同细胞类型之间的甲基化存在明显且可重复的差异。淋巴细胞DNA的甲基化水平最高,而胎盘DNA和细胞系DNA的甲基化水平较低但相似。直接测量时,Til 1的5-甲基胞嘧啶水平异常低,在所检测的任何限制酶切位点均未检测到甲基化。

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