TY - JOUR
T1 - Expression profiling using random genomic DNA microarrays identifies differentially expressed genes associated with three major developmental stages of the protozoan parasite Leishmania major
AU - Akopyants, Natalia S.
AU - Matlib, Robin S.
AU - Bukanova, Elena N.
AU - Smeds, Matthew R.
AU - Brownstein, Bernard H.
AU - Stormo, Gary D.
AU - Beverley, Stephen M.
N1 - Funding Information:
The authors thank C.T. Hott and S. MacMillan for technical support, S. Hajduk, F. Li, Y. Wang and members of our laboratories for helpful discussions, and A. Capul, D. Dobson and K. Zhang for comments on the manuscript. This work was supported by National Institutes of Health grants: NIH AI29646 (S.M.B.), HG00249 (G.D.S.) and an NIH Training Grant in Genomic Science 5 T32 HG00045 (R.S.M.). The Washington University Medical School Microarray Facility was supported by funds from the Danforth Foundation and Departments of Molecular Microbiology and Genetics. We thank the Leishmania and trypanosome genome project sequencing centers (SBRI, Sanger and TIGR) for making genomic sequence data available prior to publication, and the NIAID and Wellcome Trust for support of their work.
PY - 2004/7
Y1 - 2004/7
N2 - To complete its life cycle, protozoan parasites of the genus Leishmania undergo at least three major developmental transitions. However, previous efforts to identify genes showing stage regulated changes in transcript abundance have yielded relatively few. Here we used expression profiling to assess changes in transcript abundance in three stages: replicating promastigotes and infective non-replicating metacyclics, which occur in the sand fly vector, and in the amastigote stage residing with macrophage phagolysosomes in mammals. Microarrays were developed containing 11,484 PCR products that included a number of known genes and 10,464 random 1 kb genomic DNA fragments. Arrays were hybridized in triplicate and genes showing two-fold or greater changes in 2/3 experiments were scored as differentially expressed. Remarkably, only about one percent of the DNAs expression varied by this criteria, in either stage comparison. Northern blot analysis confirmed the predicted change in mRNA abundance for most of these (68%). This set of genes included most of those previously identified in the literature as differentially regulated as well as a number of novel genes. Notably, Leishmania maxicircle transcripts showed strong up-regulation in metacyclic and amastigote parasites, probably associated with changes in parasite energy metabolism. However, current data suggest that expression profiling using shotgun DNA libraries significantly underestimates the extent of regulated transcripts.
AB - To complete its life cycle, protozoan parasites of the genus Leishmania undergo at least three major developmental transitions. However, previous efforts to identify genes showing stage regulated changes in transcript abundance have yielded relatively few. Here we used expression profiling to assess changes in transcript abundance in three stages: replicating promastigotes and infective non-replicating metacyclics, which occur in the sand fly vector, and in the amastigote stage residing with macrophage phagolysosomes in mammals. Microarrays were developed containing 11,484 PCR products that included a number of known genes and 10,464 random 1 kb genomic DNA fragments. Arrays were hybridized in triplicate and genes showing two-fold or greater changes in 2/3 experiments were scored as differentially expressed. Remarkably, only about one percent of the DNAs expression varied by this criteria, in either stage comparison. Northern blot analysis confirmed the predicted change in mRNA abundance for most of these (68%). This set of genes included most of those previously identified in the literature as differentially regulated as well as a number of novel genes. Notably, Leishmania maxicircle transcripts showed strong up-regulation in metacyclic and amastigote parasites, probably associated with changes in parasite energy metabolism. However, current data suggest that expression profiling using shotgun DNA libraries significantly underestimates the extent of regulated transcripts.
KW - DNA microarray
KW - Expression profiling
KW - Gene expression
KW - Genome
KW - Leishmania
KW - Transcriptional regulation
UR - http://www.scopus.com/inward/record.url?scp=2342467942&partnerID=8YFLogxK
U2 - 10.1016/j.molbiopara.2004.03.002
DO - 10.1016/j.molbiopara.2004.03.002
M3 - Article
C2 - 15138069
AN - SCOPUS:2342467942
SN - 0166-6851
VL - 136
SP - 71
EP - 86
JO - Molecular and Biochemical Parasitology
JF - Molecular and Biochemical Parasitology
IS - 1
ER -