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tbnat的突变与表达分析及其对异烟肼的反应

Mutational and expression analysis of tbnat and its response to isoniazid.

作者信息

Sholto-Douglas-Vernon Carolyn, Sandy James, Victor Thomas C, Sim Edith, Helden Paul Dvan

机构信息

MRC Centre for Molecular and Cellular Biology and Department of Medical Biochemistry, University of Stellenbosch, Faculty of Health Sciences, PO Box 19063, Tygerberg, 7505, South Africa 2Department of Pharmacology, University of Oxford, Oxford, UK.

出版信息

J Med Microbiol. 2005 Dec;54(Pt 12):1189-1197. doi: 10.1099/jmm.0.46153-0.

Abstract

A gene (nat) encoding arylamine N-acetyltransferase (NAT) has been found in Mycobacterium tuberculosis. The gene is expressed and the enzyme is active in growing M. tuberculosis cells. N-Acetyltransferase acetylates and inactivates isoniazid (INH), which is a front-line drug used in tuberculosis (TB) therapy. In this study, it was shown that a previously reported G619A single nucleotide polymorphism (SNP) was conserved in two M. tuberculosis strain families found in the Western Cape Province of South Africa (strain families 3 and 28). Further sequence analysis of isolates in strain family 3 identified a new T529C SNP in NAT resulting in a histidine instead of a tyrosine at position 177. This SNP was found only in isolates from strain family 3, and this mutation affects the highly conserved tyrosine residue close to the active site. Using real-time PCR, the expression of M. tuberculosis nat (tbnat) was determined over a 28 day growth cycle of the M. tuberculosis reference strain (H37Rv). The expression of tbnat occurs early in growth and reaches maximum levels at mid-exponential phase. The exposure of INH-susceptible isolates to low levels of INH resulted in an increase of tbnat expression (reference strain H37Rv, which is wild-type for tbnat, and isolate 1430, containing both SNPs). An INH-resistant isolate (816) exposed to INH showed no change in tbnat expression. The increased expression in the susceptible isolates suggests that INH affects tbnat expression. tbnat may contribute to INH susceptibility, but in combination with other factors.

摘要

在结核分枝杆菌中发现了一个编码芳胺N - 乙酰转移酶(NAT)的基因(nat)。该基因可表达,且该酶在生长的结核分枝杆菌细胞中具有活性。N - 乙酰转移酶可使异烟肼(INH)乙酰化并使其失活,而异烟肼是结核病(TB)治疗中使用的一线药物。在本研究中,结果表明,先前报道的G619A单核苷酸多态性(SNP)在南非西开普省发现的两个结核分枝杆菌菌株家族(菌株家族3和28)中是保守的。对菌株家族3中的分离株进行进一步的序列分析,在NAT中鉴定出一个新的T529C SNP,导致第177位的组氨酸取代了酪氨酸。该SNP仅在菌株家族3的分离株中发现,并且此突变影响了靠近活性位点的高度保守的酪氨酸残基。使用实时PCR,在结核分枝杆菌参考菌株(H37Rv)的28天生长周期内测定了结核分枝杆菌nat(tbnat)的表达。tbnat的表达在生长早期出现,并在指数中期达到最高水平。将对INH敏感的分离株暴露于低水平的INH会导致tbnat表达增加(参考菌株H37Rv,其tbnat为野生型,以及分离株1430,包含两个SNP)。暴露于INH的耐INH分离株(816)的tbnat表达没有变化。敏感分离株中表达的增加表明INH影响tbnat表达。tbnat可能有助于INH敏感性,但需与其他因素共同作用。

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