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鉴定和表征参与米曲霉分生孢子发育早期的一个假定碱性螺旋-环-螺旋转录因子。

Identification and characterization of a putative basic helix-loop-helix transcription factor involved in the early stage of conidiophore development in Aspergillus oryzae.

机构信息

Noda Institute for Scientific Research, 399 Noda, Noda City 278-0037, Japan.

出版信息

Fungal Genet Biol. 2011 Dec;48(12):1108-15. doi: 10.1016/j.fgb.2011.10.001. Epub 2011 Oct 10.

Abstract

The helix-loop-helix (HLH) family of transcriptional factors is a key player in a wide range of developmental processes. HLH proteins form homo- and/or heterodimers with other HLH proteins and bind to E-box motifs. The regulation and functions of these proteins can be complex due to their bifunctional roles as activators and repressors of gene transcription. In this study, we isolated and characterized a novel predicted bHLH protein-encoding gene, AO090023000902, designated ecdR (early conidiophore development regulator), in Aspergillus oryzae. The ecdR gene disruptant produced very few conidia. Conversely, the overexpression of ecdR resulted in the formation of a large number of conidia at an early stage, suggesting that the EcdR protein is required for early asexual development. Additionally, when serially diluted conidia were spread-cultivated onto malt agar medium, we found that conidial number of the control strain depended on the cultivated conidium density, while the ecdR-overexpressing strain showed no significant change in conidiation. These phenotypes of ecdR-disruptant and ecdR-overexpressing strains are partially similar to those of the sclR-overexpressing strain and sclR-disruptant, respectively. Yeast two-hybrid assays and sclR, ecdR-double deletion experiment indicated that EcdR plays a major role in conidiation, and SclR represses this function by competitively interacting with EcdR in A. oryzae.

摘要

螺旋-环-螺旋转录因子(HLH)家族是广泛发育过程中的关键因子。HLH 蛋白与其他 HLH 蛋白形成同源和/或异源二聚体,并与 E 盒基序结合。由于其作为基因转录的激活剂和抑制剂的双重功能,这些蛋白质的调节和功能可能很复杂。在这项研究中,我们在米曲霉中分离并鉴定了一个新的预测 bHLH 蛋白编码基因,命名为 ecdR(早期分生孢子发育调节剂)。ecdR 基因缺失突变体产生的分生孢子非常少。相反,ecdR 的过表达导致在早期形成大量分生孢子,表明 EcdR 蛋白是早期无性发育所必需的。此外,当连续稀释的分生孢子铺在麦芽琼脂培养基上进行扩散培养时,我们发现对照菌株的分生孢子数取决于培养的分生孢子密度,而 ecdR 过表达菌株的分生能力没有显著变化。ecdR 缺失突变体和 ecdR 过表达菌株的这些表型与 sclR 过表达菌株和 sclR 缺失突变体的表型分别有些相似。酵母双杂交测定和 sclR、ecdR 双缺失实验表明,EcdR 在分生孢子形成中起主要作用,而 SclR 通过与 A.oryzae 中的 EcdR 竞争相互作用来抑制该功能。

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