Pathway Activity Profiling (PAPi): from the metabolite profile to the metabolic pathway activity

被引:103
作者
Aggio, Raphael B. M. [1 ]
Ruggiero, Katya [1 ]
Villas-Boas, Silas Granato [1 ]
机构
[1] Univ Auckland, Sch Biol Sci, Auckland 1142, New Zealand
关键词
BIOLOGY;
D O I
10.1093/bioinformatics/btq567
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Motivation: Metabolomics is one of the most recent omics-technologies and uses robust analytical techniques to screen low molecular mass metabolites in biological samples. It has evolved very quickly during the last decade. However, metabolomics datasets are considered highly complex when used to relate metabolite levels to metabolic pathway activity. Despite recent developments in bioinformatics, which have improved the quality of metabolomics data, there is still no straightforward method capable of correlating metabolite level to the activity of different metabolic pathways operating within the cells. Thus, this kind of analysis still depends on extremely laborious and time-consuming processes. Results: Here, we present a new algorithm Pathway Activity Profiling (PAPi) with which we are able to compare metabolic pathway activities from metabolite profiles. The applicability and potential of PAPi was demonstrated using a previously published data from the yeast Saccharomyces cerevisiae. PAPi was able to support the biological interpretations of the previously published observations and, in addition, generated new hypotheses in a straightforward manner. However, PAPi is time consuming to perform manually. Thus, we also present here a new R-software package (PAPi) which implements the PAPi algorithm and facilitates its usage to quickly compare metabolic pathways activities between different experimental conditions. Using the identified metabolites and their respective abundances as input, the PAPi package calculates pathways' Activity Scores, which represents the potential metabolic pathways activities and allows their comparison between conditions. PAPi also performs principal components analysis and analysis of variance or t-test to investigate differences in activity level between experimental conditions. In addition, PAPi generates comparative graphs highlighting up-and down-regulated pathway activity.
引用
收藏
页码:2969 / 2976
页数:8
相关论文
共 21 条
[1]
Current status of systems biology in Aspergilli [J].
Andersen, M. R. ;
Nielsen, J. .
FUNGAL GENETICS AND BIOLOGY, 2009, 46 :S180-S190
[2]
Arita Masanori, 2004, Briefings in Functional Genomics & Proteomics, V3, P84, DOI 10.1093/bfgp/3.1.84
[3]
Integration of metabolome data with metabolic networks reveals reporter reactions [J].
Cakir, Tunahan ;
Patil, Kiran Raosaheb ;
Onsan, Zeynep ILsen ;
Ulgen, Kutlu Ozergin ;
Kirdar, Betul ;
Nielsen, Jens .
MOLECULAR SYSTEMS BIOLOGY, 2006, 2 (1)
[4]
Carlson M, 2009, KEGG DB SET ANNOTATI
[5]
Current trends and future requirements for the mass spectrometric investigation of microbial, mammalian and plant metabolomes [J].
Dunn, Warwick B. .
PHYSICAL BIOLOGY, 2008, 5 (01)
[6]
Bioconductor: open software development for computational biology and bioinformatics [J].
Gentleman, RC ;
Carey, VJ ;
Bates, DM ;
Bolstad, B ;
Dettling, M ;
Dudoit, S ;
Ellis, B ;
Gautier, L ;
Ge, YC ;
Gentry, J ;
Hornik, K ;
Hothorn, T ;
Huber, W ;
Iacus, S ;
Irizarry, R ;
Leisch, F ;
Li, C ;
Maechler, M ;
Rossini, AJ ;
Sawitzki, G ;
Smith, C ;
Smyth, G ;
Tierney, L ;
Yang, JYH ;
Zhang, JH .
GENOME BIOLOGY, 2004, 5 (10)
[7]
Ihaka R., 1996, J. Comput. Graph. Stat., V5, P299, DOI [10.2307/1390807, 10.1080/10618600.1996.10474713, DOI 10.1080/10618600.1996.10474713]
[8]
GMD@CSB.DB:: the Golm Metabolome Database [J].
Kopka, J ;
Schauer, N ;
Krueger, S ;
Birkemeyer, C ;
Usadel, B ;
Bergmüller, E ;
Dörmann, P ;
Weckwerth, W ;
Gibon, Y ;
Stitt, M ;
Willmitzer, L ;
Fernie, AR ;
Steinhauser, D .
BIOINFORMATICS, 2005, 21 (08) :1635-1638
[9]
Lemon J., 2010, R-news, V6, P8
[10]
The next wave in metabolome analysis [J].
Nielsen, J ;
Oliver, S .
TRENDS IN BIOTECHNOLOGY, 2005, 23 (11) :544-546