Rautengarten Carsten, Steinhauser Dirk, Büssis Dirk, Stintzi Annick, Schaller Andreas, Kopka Joachim, Altmann Thomas
Institut für Biochemie und Biologie, Genetik, Universität Potsdam, Golm, Germany.
PLoS Comput Biol. 2005 Sep;1(4):e40. doi: 10.1371/journal.pcbi.0010040. Epub 2005 Sep 23.
The gene family of subtilisin-like serine proteases (subtilases) in Arabidopsis thaliana comprises 56 members, divided into six distinct subfamilies. Whereas the members of five subfamilies are similar to pyrolysins, two genes share stronger similarity to animal kexins. Mutant screens confirmed 144 T-DNA insertion lines with knockouts for 55 out of the 56 subtilases. Apart from SDD1, none of the confirmed homozygous mutants revealed any obvious visible phenotypic alteration during growth under standard conditions. Apart from this specific case, forward genetics gave us no hints about the function of the individual 54 non-characterized subtilase genes. Therefore, the main objective of our work was to overcome the shortcomings of the forward genetic approach and to infer alternative experimental approaches by using an integrative bioinformatics and biological approach. Computational analyses based on transcriptional co-expression and co-response pattern revealed at least two expression networks, suggesting that functional redundancy may exist among subtilases with limited similarity. Furthermore, two hubs were identified, which may be involved in signalling or may represent higher-order regulatory factors involved in responses to environmental cues. A particular enrichment of co-regulated genes with metabolic functions was observed for four subtilases possibly representing late responsive elements of environmental stress. The kexin homologs show stronger associations with genes of transcriptional regulation context. Based on the analyses presented here and in accordance with previously characterized subtilases, we propose three main functions of subtilases: involvement in (i) control of development, (ii) protein turnover, and (iii) action as downstream components of signalling cascades. Supplemental material is available in the Plant Subtilase Database (PSDB) (http://csbdb.mpimp-golm.mpg.de/psdb.html), as well as from the CSB.DB (http://csbdb.mpimp-golm.mpg.de).
拟南芥中枯草杆菌蛋白酶样丝氨酸蛋白酶(枯草杆菌蛋白酶)基因家族由56个成员组成,分为六个不同的亚家族。其中五个亚家族的成员与热解素相似,而有两个基因与动物凯欣蛋白的相似性更强。突变体筛选确定了144个T-DNA插入系,这些插入系导致56个枯草杆菌蛋白酶中的55个基因敲除。除了SDD1之外,在标准条件下生长期间,没有一个已确认的纯合突变体显示出任何明显的可见表型改变。除了这个特殊情况外,正向遗传学没有为我们提供有关54个未表征的枯草杆菌蛋白酶基因功能的任何线索。因此,我们工作的主要目标是克服正向遗传方法的缺点,并通过使用综合生物信息学和生物学方法推断替代实验方法。基于转录共表达和共响应模式的计算分析揭示了至少两个表达网络,这表明相似性有限的枯草杆菌蛋白酶之间可能存在功能冗余。此外,还鉴定出两个枢纽,它们可能参与信号传导,或者可能代表参与对环境线索响应的高阶调节因子。对于四个可能代表环境胁迫晚期响应元件的枯草杆菌蛋白酶,观察到具有代谢功能的共调控基因有特别富集的现象。凯欣同源物与转录调控背景的基因有更强的关联。基于此处给出的分析并根据先前表征的枯草杆菌蛋白酶,我们提出枯草杆菌蛋白酶的三个主要功能:参与(i)发育控制,(ii)蛋白质周转,以及(iii)作为信号级联的下游组分起作用。补充材料可在植物枯草杆菌蛋白酶数据库(PSDB)(http://csbdb.mpimp-golm.mpg.de/psdb.html)以及CSB.DB(http://csbdb.mpimp-golm.mpg.de)中获得。