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丁酸盐和乙酰肉碱在体外可抑制脆性X染色体的细胞遗传学表达。

Butyrate and acetyl-carnitine inhibit the cytogenetic expression of the fragile X in vitro.

作者信息

Pomponi M G, Neri G

机构信息

Istituto di Genetica Medica, Facoltà di Medicina A. Gemelli, Università Cattolica, Rome, Italy.

出版信息

Am J Med Genet. 1994 Jul 15;51(4):447-50. doi: 10.1002/ajmg.1320510428.

Abstract

Cytogenetic expression of the fragile site at Xq27.3 is only found in those patients who have a full mutation of the FMR1 gene, i.e., a large amplification of the CGG repeat. However, an expansion of this repeat, although necessary, does not seem to be sufficient to cause expression of fra(X)(q27.3). Other factors are clearly needed, e.g., thymidylate stress. Little or no attention has been paid to the possible role of histones in the expression of the fragile sites, in spite of their structural and regulatory role in the chromatin complex. Histones can be modified by treating intact cells in vitro with butyrate, a substance that causes histone acetylation. The purpose of the present work is to test the effect of butyrate and of the acetylating compound acetyl-L-carnitine on the expression of fra(X)(q27.3) by treating peripheral lymphocytes of fragile X syndrome patients with these substances in vitro. We show that this treatment causes a significant inhibition of fra(X)(q27.3) expression.

摘要

Xq27.3脆性位点的细胞遗传学表达仅在那些FMR1基因发生完全突变的患者中发现,即CGG重复序列的大量扩增。然而,这种重复序列的扩增虽然是必要的,但似乎不足以导致fra(X)(q27.3)的表达。显然还需要其他因素,例如胸苷酸应激。尽管组蛋白在染色质复合物中具有结构和调节作用,但很少或根本没有关注其在脆性位点表达中的可能作用。可以通过在体外使用丁酸盐处理完整细胞来修饰组蛋白,丁酸盐是一种可导致组蛋白乙酰化的物质。本研究的目的是通过在体外使用这些物质处理脆性X综合征患者的外周淋巴细胞,来测试丁酸盐和乙酰化化合物乙酰-L-肉碱对fra(X)(q27.3)表达的影响。我们发现这种处理可显著抑制fra(X)(q27.3)的表达。

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