Adler Chen, Segal Gil
The Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv-Yafo, Israel.
mBio. 2025 Jul 9;16(7):e0126825. doi: 10.1128/mbio.01268-25. Epub 2025 May 30.
The intracellular pathogen utilizes the Icm/Dot type IVB secretion system, which translocates >300 effector proteins into host cells. The expression of the effector-encoding genes (EEGs) is mediated by a combination of global and local transcriptional regulators. Here, we describe two novel LysR-type transcriptional regulators (LTTRs), LelB (lpg2138) and LelC (lpg1796), which function as local regulators of EEG in . Bioinformatic analysis, expression assays, site-directed mutagenesis, and binding experiments led to the discovery that in LelB controls the expression of three EEGs, and LelC controls the expression of a single EEG. Moreover, we discovered a versatile regulator, LelB, that can serve either as a global or local regulator of EEGs. The LelB orthologs in the genus are divided into three clades, but only in two of them is located adjacent to its target genes and functions as a local regulator. A genomic search using the validated LelB regulatory element identified multiple genes (between 19 and 36) harboring the LelB regulatory element in the five species belonging to the third clade. Examination of this collection of genes uncovered that most of them harbor common effector domains and other known effector features. Furthermore, experimental analysis of these genes from one of these species, , indicated that LelB regulates their expression. Our results demonstrate that LelB functions as a local or global regulator of EEGs in different species, thus uncovering the remarkable versatility of effector regulation by LTTRs in the genus.
translocates into host cells the largest number of effector proteins known in any pathogen. This cohort of proteins needs to be coordinated at the gene expression level to result in a successful infection. To date, the regulation of effector-encoding genes in has been found to be mediated by global regulators that control the expression of multiple effectors and local regulators that control the expression of a single or few effectors. Here, we identified two novel regulators that function as local regulators of effectors in . However, analysis of their orthologs across the genus revealed that one of them controls the expression of multiple genes in five species. The properties of the proteins encoded by these genes suggest that most of them function as effectors. Our data demonstrate a versatile regulator whose orthologs function as local or global regulators of EEGs in different species.
细胞内病原体利用Icm/Dot IVB型分泌系统,该系统可将300多种效应蛋白转运到宿主细胞中。效应蛋白编码基因(EEGs)的表达由全局和局部转录调节因子共同介导。在此,我们描述了两种新型的LysR型转录调节因子(LTTRs),即LelB(lpg2138)和LelC(lpg1796),它们在[具体物种]中作为EEGs的局部调节因子发挥作用。生物信息学分析、表达测定、定点诱变和[具体结合实验名称]实验导致发现,在[具体物种]中LelB控制三个EEGs的表达,而LelC控制单个EEG的表达。此外,我们发现了一种多功能调节因子LelB,它既可以作为EEGs的全局调节因子,也可以作为局部调节因子。[具体物种属]中的LelB直系同源物分为三个进化枝,但只有其中两个进化枝中的[具体基因或元件]位于其靶基因附近并作为局部调节因子发挥作用。使用经过验证的LelB调节元件进行基因组搜索,在属于第三个进化枝的五个[具体物种]中鉴定出多个(19至36个)含有LelB调节元件的基因。对这些基因集合的研究发现,它们中的大多数都具有共同的效应结构域和其他已知的效应特征。此外,对来自这些物种之一[具体物种名称]的这些基因的实验分析表明,LelB调节它们的表达。我们的结果表明,LelB在不同的[具体物种]中作为EEGs的局部或全局调节因子发挥作用,从而揭示了LTTRs在[具体物种属]中效应调节的显著多功能性。
[具体病原体名称]向宿主细胞转运的效应蛋白数量是任何病原体中已知最多的。这一组蛋白需要在基因表达水平上进行协调,以实现成功感染。迄今为止,已发现[具体病原体名称]中效应蛋白编码基因的调节由控制多种效应蛋白表达的全局调节因子和控制单个或少数效应蛋白表达的局部调节因子介导。在此,我们鉴定了两种新型调节因子,它们在[具体物种]中作为效应蛋白的局部调节因子发挥作用。然而,对它们在[具体物种属]中的直系同源物的分析表明,其中一个在五个[具体物种]中控制多个基因的表达。这些基因编码的蛋白质的特性表明,它们中的大多数作为效应蛋白发挥作用。我们的数据证明了一种多功能调节因子,其直系同源物在不同[具体物种]中作为EEGs的局部或全局调节因子发挥作用。