Suppr超能文献

合成信息素对[具体对象]交配信息素反应途径的激活。 (注:原文中“of by”表述有误,推测完整可能是“Activation of the Mating Pheromone Response Pathway of [具体对象] by Synthetic Pheromones” )

Activation of the Mating Pheromone Response Pathway of by Synthetic Pheromones.

作者信息

Ha Byeongsuk, Kim Sinil, Kim Minseek, Ro Hyeon-Su

机构信息

Division of Applied Life Science and Research Institute of Life Sciences, Gyeongsang National University, Jinju, Korea.

出版信息

Mycobiology. 2018 Dec 21;46(4):407-415. doi: 10.1080/12298093.2018.1541518. eCollection 2018.

Abstract

Pheromone (PHB)-receptor (RCB) interaction in the mating pheromone response pathway of was investigated using synthetic PHBs. Functionality of the C-terminally carboxymethylated synthetic PHBs was demonstrated by concentration-dependent induction of a mating-related gene () expression and by pseudoclamp formation in a monokaryotic strain S1-11 of . Treatment with synthetic PHBs activated the expression of homeodomain genes (s) residing in the mating type locus, and of -regulated genes, including , , and , as well as genes in the mating type locus, including pheromone () and receptor () genes. The synthetic PHBs failed to discriminate self from non-self RCBs. PHBs of the mating type ( PHBs) were able to activate the mating pheromone response pathway in both monokaryotic S1-11 and S1-13 strains, whose mating types were (self) and (non-self), respectively. The same was true for PHBs in the (non-self) and (self) mating types. The synthetic PHBs also promoted the mating of two monokaryotic strains carrying -common incompatible mating types ( ×). However, the dikaryon generated by this process exhibited abnormally high content of hyphal branching and frequent clamp connections and, more importantly, was found to be genetically unstable due to overexpression of mating-related genes such as . Although synthetic PHBs were unable to discriminate self from non-self RCBs, they showed a higher affinity for non-self RCBs, through which the mating pheromone response pathway in non-self cells may be preferentially activated.

摘要

利用合成信息素研究了[具体物种]交配信息素反应途径中信息素(PHB)-受体(RCB)的相互作用。通过浓度依赖性诱导交配相关基因([具体基因])表达以及在[具体物种]的单核菌株S1-11中形成假夹,证明了C末端羧甲基化合成信息素的功能。用合成信息素处理激活了位于[具体物种]交配型位点的同源结构域基因([具体基因])以及包括[具体基因1]、[具体基因2]和[具体基因3]在内的[具体调控基因]调控的基因,以及交配型位点中的基因,包括信息素([具体信息素基因])和受体([具体受体基因])基因。合成信息素无法区分自身和非自身的RCB。[具体交配型]的信息素([具体交配型PHB])能够激活单核S1-11和S1-13菌株中的交配信息素反应途径,这两个菌株[具体交配型]分别为[自身交配型](自身)和[非自身交配型](非自身)。对于[另一种交配型](非自身)和[另一种交配型](自身)交配型中的[具体交配型PHB]也是如此。合成信息素还促进了携带[具体共同不相容交配型]([具体交配型组合])的两个单核菌株的交配。然而,由此产生的双核体表现出异常高的菌丝分支含量和频繁的夹状连接,更重要的是,由于[具体交配相关基因]等交配相关基因的过度表达,发现其遗传不稳定。尽管合成信息素无法区分自身和非自身的RCB,但它们对非自身RCB表现出更高的亲和力,通过这种亲和力,非自身细胞中的交配信息素反应途径可能被优先激活。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验