Deconvolving cell cycle expression data with complementary information

被引:39
作者
Bar-Joseph, Ziv [1 ]
Farkash, Shlomit [2 ]
Gifford, David K. [3 ]
Simon, Itamar [2 ]
Rosenfeld, Roni [1 ]
机构
[1] Carnegie Mellon Univ, Sch Comp Sci, Pittsburgh, PA 15213 USA
[2] Hebrew Univ Jerusalem, Sch Med, IL-91120 Jerusalem, Israel
[3] MIT CSAIL, Cambridge, MA 02139 USA
关键词
D O I
10.1093/bioinformatics/bth915
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: In the study of many systems, cells are first synchronized so that a large population of cells exhibit similar behavior. While synchronization can usually be achieved for a short duration, after a while cells begin to lose their synchronization. Synchronization loss is a continuous process and so the observed value in a population of cells for a gene at time t is actually a convolution of its values in an interval around t. Deconvolving the observed values from a mixed population will allow us to obtain better models for these systems and to accurately detect the genes that participate in these systems. Results: We present an algorithm which combines budding index and gene expression data to deconvolve expression profiles. Using the budding index data we first fit a synchronization loss model for the cell cycle system. Our deconvolution algorithm uses this loss model and can also use information from co-expressed genes, making it more robust against noise and missing values. Using expression and budding data for yeast we show that our algorithm is able to reconstruct a more accurate representation when compared with the observed values. In addition, using the deconvolved profiles we are able to correctly identify 15% more cycling genes when compared to a set identified using the observed values.
引用
收藏
页码:23 / 30
页数:8
相关论文
共 14 条
[1]   Comparing the continuous representation of time-series expression profiles to identify differentially expressed genes [J].
Bar-Joseph, Z ;
Gerber, G ;
Simon, L ;
Gifford, DK ;
Jaakkola, TS ;
Jaakkola, TS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (18) :10146-10151
[2]  
Bar-Joseph Z., 2002, P 6 ANN INT C COMP B, P39, DOI DOI 10.1145/565196.565202
[3]   A genome-wide transcriptional analysis of the mitotic cell cycle [J].
Cho, RJ ;
Campbell, MJ ;
Winzeler, EA ;
Steinmetz, L ;
Conway, A ;
Wodicka, L ;
Wolfsberg, TG ;
Gabrielian, AE ;
Landsman, D ;
Lockhart, DJ ;
Davis, RW .
MOLECULAR CELL, 1998, 2 (01) :65-73
[4]  
CREANOR J, 1994, J CELL SCI, V107, P1197
[5]   Expression deconvolution: A reinterpretation of DNA microarray data reveals dynamic changes in cell populations [J].
Lu, P ;
Nakorchevskiy, A ;
Marcotte, EM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (18) :10370-10375
[6]   Statistical resynchronization and Bayesian detection of periodically expressed genes [J].
Lu, X ;
Zhang, W ;
Qin, ZHS ;
Kwast, KE ;
Liu, JS .
NUCLEIC ACIDS RESEARCH, 2004, 32 (02) :447-455
[7]   Coordinated transcription of key pathways in the mouse by the circadian clock [J].
Panda, S ;
Antoch, MP ;
Miller, BH ;
Su, AI ;
Schook, AB ;
Straume, M ;
Schultz, PG ;
Kay, SA ;
Takahashi, JS ;
Hogenesch, JB .
CELL, 2002, 109 (03) :307-320
[8]   Analysis of cell-cycle gene expression in Saccharomyces cerevisiae using microarrays and multiple synchronization methods [J].
Shedden, K ;
Cooper, S .
NUCLEIC ACIDS RESEARCH, 2002, 30 (13) :2920-2929
[9]   Analysis of cell-cycle-specific gene expression in human cells as determined by microarrays and double-thymidine block synchronization [J].
Shedden, K ;
Cooper, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (07) :4379-4384
[10]   Comprehensive identification of cell cycle-regulated genes of the yeast Saccharomyces cerevisiae by microarray hybridization [J].
Spellman, PT ;
Sherlock, G ;
Zhang, MQ ;
Iyer, VR ;
Anders, K ;
Eisen, MB ;
Brown, PO ;
Botstein, D ;
Futcher, B .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (12) :3273-3297