TY - JOUR
T1 - Neomycin and puromycin affect gene expression in Giardia lamblia stable transfection
AU - Su, Li Hsin
AU - Lee, Gilbert A.
AU - Huang, Yu Chang
AU - Chen, Yi Hsiu
AU - Sun, Chin Hung
N1 - Funding Information:
This work was supported by grants from the National Science Council (NSC 94-2320-B-002-093) and the National Health Research Institutes (NHRI-EX95-9510NC and NHRI-EX96-9510NC) in Taiwan and was also supported in part by the Department of Medical Research in NTUH. We thank the researchers and administrators of the G. lamblia Genome database. We thank Dr. Gaetan Fauber for providing us mouse anti-CWP2 monoclonal antibody. We also thank Dr. Zee-Fen Chang and Ms Sui-Chih Tien for their valuable help with the 2D gel analysis.
Copyright:
Copyright 2009 Elsevier B.V., All rights reserved.
PY - 2007/12
Y1 - 2007/12
N2 - Two systems for stable transfection of Giardia have been established using selection either by neomycin or by puromycin. We asked if these selection systems themselves influenced expression of endogenous giardial genes. Northern blot analysis showed a ∼1.4 to ∼7-fold increase in the encystation-induced cyst wall protein 1 (cwp1), cwp2, and gmyb2 gene transcripts in the drug selected cell lines during vegetative growth, compared with untransfected cells. However, the levels of the constitutive ran, lrp3, or α2-tubulin gene transcripts decreased slightly or did not change in these stably transfected cell lines. Part of the effect could be due to drug selection, since treatment of untransfected cells with G418 or puromycin also had similar effects. Nuclear run-on assays showed that part of the effect comes from an increase in transcription initiation rate. The levels of CWP and cyst formation during vegetative growth also increased in the transfected cell lines. Using proteomic technologies, we identified eight genes whose expression is upregulated in neomycin selected cell lines, including phosphoglycerate kinase, glyceraldehyde-3-phosphate dehydrogenase, ornithine carbamoyltransferase, carbamate kinase, orf 16424, cyclophilin, co-chaperone-like p21, and bip. Six of these are also upregulated in puromycin selected cell lines. Our results indicate that transfection and drug selection, per se, can alter expression of genes involved in metabolism, protein folding, and differentiation status in Giardia.
AB - Two systems for stable transfection of Giardia have been established using selection either by neomycin or by puromycin. We asked if these selection systems themselves influenced expression of endogenous giardial genes. Northern blot analysis showed a ∼1.4 to ∼7-fold increase in the encystation-induced cyst wall protein 1 (cwp1), cwp2, and gmyb2 gene transcripts in the drug selected cell lines during vegetative growth, compared with untransfected cells. However, the levels of the constitutive ran, lrp3, or α2-tubulin gene transcripts decreased slightly or did not change in these stably transfected cell lines. Part of the effect could be due to drug selection, since treatment of untransfected cells with G418 or puromycin also had similar effects. Nuclear run-on assays showed that part of the effect comes from an increase in transcription initiation rate. The levels of CWP and cyst formation during vegetative growth also increased in the transfected cell lines. Using proteomic technologies, we identified eight genes whose expression is upregulated in neomycin selected cell lines, including phosphoglycerate kinase, glyceraldehyde-3-phosphate dehydrogenase, ornithine carbamoyltransferase, carbamate kinase, orf 16424, cyclophilin, co-chaperone-like p21, and bip. Six of these are also upregulated in puromycin selected cell lines. Our results indicate that transfection and drug selection, per se, can alter expression of genes involved in metabolism, protein folding, and differentiation status in Giardia.
KW - Giardia
KW - Neomycin
KW - Puromycin
KW - Transfection
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U2 - 10.1016/j.molbiopara.2007.07.015
DO - 10.1016/j.molbiopara.2007.07.015
M3 - Article
C2 - 17765984
AN - SCOPUS:35348969738
SN - 0166-6851
VL - 156
SP - 124
EP - 135
JO - Molecular and Biochemical Parasitology
JF - Molecular and Biochemical Parasitology
IS - 2
ER -