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肝片吸虫:通过差异显示鉴定的新基因序列的阶段特异性表达

Fasciola hepatica: stage-specific expression of novel gene sequences as identified by differential display.

作者信息

Reed M B, Spithill T W, Strugnell R A, Panaccio M

机构信息

Victorian Institute of Animal Science, Attwood, Australia.

出版信息

Exp Parasitol. 1998 Jun;89(2):169-79. doi: 10.1006/expr.1998.4287.

Abstract

Differences in gene expression between adult and immature Fasciola hepatica (liver fluke) parasites isolated from the mammalian host were investigated using the technique of differential display. For any given primer combination used to produce these displays there were, on average, 22% apparently adult-specific and 14% apparently immature-specific cDNA products able to be identified, consistent with a high degree of differential gene expression between these two parasite developmental stages. Several cDNA fragments specific to immature parasite RNA were isolated and cloned. An abundant 400- to 500-bp RNA species was identified on a Northern blot by hybridization to the cloned DD2 cDNA fragment and was determined to be expressed at levels at least 10-fold higher in immature parasites relative to adult parasites. mRNA transcripts corresponding to the remaining cDNA fragments (DD14, DD16, DISP10, and DISP2) were apparently expressed at levels below the sensitivity limits of Northern analysis, although differential expression of these transcripts was confirmed by reverse transcriptase PCR (RT-PCR). The identities or functional significance of each of the five differentially expressed cDNAs identified in this study is still unclear due to the lack of any significant sequence similarity to the entries currently held within sequence databases.

摘要

利用差异显示技术研究了从哺乳动物宿主中分离出的成年和未成熟肝片吸虫(肝吸虫)寄生虫之间的基因表达差异。对于用于产生这些显示的任何给定引物组合,平均有22%明显为成年特异性和14%明显为未成熟特异性的cDNA产物能够被鉴定出来,这与这两个寄生虫发育阶段之间高度的差异基因表达一致。分离并克隆了几个未成熟寄生虫RNA特有的cDNA片段。通过与克隆的DD2 cDNA片段杂交,在Northern印迹上鉴定出一种丰富的400至500bp的RNA种类,并确定其在未成熟寄生虫中的表达水平相对于成年寄生虫至少高10倍。对应于其余cDNA片段(DD14、DD16、DISP10和DISP2)的mRNA转录本在Northern分析的灵敏度极限以下表达,尽管这些转录本的差异表达通过逆转录酶PCR(RT-PCR)得到了证实。由于与序列数据库中目前保存的条目缺乏任何显著的序列相似性,本研究中鉴定出的五个差异表达cDNA中每一个的身份或功能意义仍不清楚。

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