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Copyright ©The Author(s) 2015.
World J Gastroenterol. Nov 14, 2015; 21(42): 12042-12058
Published online Nov 14, 2015. doi: 10.3748/wjg.v21.i42.12042
Table 1 Advantages and disadvantages of constitutive and inducible expression systems
Expression systemsAdvantagesDisadvantages
ConstitutiveWell established, commercially available; in vitro and in vivo, successful methodology for expression of transgeneExpression of oncogenes may cause advanced/highly aggressive tumors and early lethality
Heat-shockExpression of transgene can be induced on a single cell levelAdverse effects that may arise from the heat shock
Cre-loxPWell established; commercially available; in vivo, successful methodology for expression of transgeneNot all tissue specific promoters are perfectly specific; leaky gene expression; two plasmid system
GAL4/UASWell established; in vivo, successful methodology for expression of transgeneIn vivo expression of GAL4 can have side effects, probably related to immune and stress responses; two plasmid system
MifepristoneWell established; in vivo, successful methodology for expression of transgeneOpening and closing of the switch is slow (hours to days); cell permeability of the RU-486 can be restricted
Tet-on/off-inducibleWell established; commercially available; in vitro and in vivo, successful methodology for expression of transgeneOpening and closing of the switch is slow (hours to days); cell permeability of the doxycycline can be restricted; two plasmid system
Table 2 Characteristics of three genome editing systems
NucleasesZFNTALENCRISPR/Cas
DNA binding domainMultiple zinc finger peptidesTranscription-activator like effectorsCRISPR-derived RNA/Single-guide RNA
EndonucleaseFok1Fok1Cas9
Binding specificity of each repeat3 bp2 bp1 bp
Target site length18 to 36 bp30 to 40 bp23 bp
Off-targetHigh probabilityLow probabilityVariable
Libraries generationNoFeasible, depend on technologyYes, cloning 20 bp, oligos targeting each gene into a plasmid
Table 3 Zebrafish animal models of liver disease and hepatocellular carcinoma
Transgene nameExpression systemLiver pathologyRef.
cnr1 (Zebrafish)Tet-off-inducibleSteatosis[132]
edn1 (Zebrafish)ConstitutiveSteatosis, bile duct dilation, hyperplasia and HCC[69]
gankyrin (Zebrafish)ConstitutiveAtrophy, hypoplasia and steatosis[123]
HBx (Human)ConstitutiveHypoplasia and steatosis[120]
HBx + AFB1 (Human)ConstitutiveHepatitis, steatosis and hyperplasia[134]
HBx + HCV (Human)Tet-off-inducibleIntrahepatic cholangiocarcinoma[81]
HBx + p53M214 (Human)ConstitutiveChronic inflammation, steatosis, bile duct dilation, dysplasia and HCC[70]
HBx + src (Human/Zebrafish)ConstitutiveChronic inflammation, steatosis, bile duct dilation, dysplasia and HCC[70]
HCV (Human)ConstitutiveSteatosis[29]
HCV + TAA (Human)ConstitutiveSteatosis and HCC[29]
kras-G12V (Zebrafish)MifepristoneHyperplasia and HCC[82]
kras-G12V (Zebrafish)ConstitutiveHyperplasia and hepatocellular adenoma[82]
kras-G12V (Zebrafish)Tet-on-inducibleHyperplasia, hepatocellular adenoma and HCC[137]
kras-G12V + p53M214 (Zebrafish)ConstitutiveHyperplasia and hepatocellular adenoma[82]
kras-G12V + RhoA (Zebrafish)Tet-on-inducibleHyperplasia, hepatocellular adenoma and HCC[137]
kras-G12V + RhoAG14V (Zebrafish)Tet-on-inducibleHyperplasia, hepatocellular adenoma and HCC[137]
kras-G12V + RhoAT19N (Zebrafish)Tet-on-inducibleHCC[137]
Lc3 (Rat)ConstitutiveInvestigation of liver autophagy[141]
mdm2 (Zebrafish)ConstitutiveAtrophy, contraction and hypoplasia[121]
MYC (Mouse)Tet-on-inducibleHyperplasia and hepatocellular adenoma[83]
myca (Zebrafish)MifepristoneSmall, typical, hypervascular and ascites of liver tumor[143]
myca + p53M214 (Zebrafish)MifepristoneSmall, typical, hypervascular and ascites of liver tumor[143]
mycb (Zebrafish)MifepristoneSmall, typical, hypervascular and ascites of liver tumor[143]
orf A (Human)GAL4/UASDelayed onset of liver tumor[79]
src (Zebrafish)ConstitutiveChronic inflammation, steatosis, bile duct dilation, hyperplasia, dysplasia and HCC[70]
src + p53M214 (Zebrafish)ConstitutiveSteatosis, hyperplasia, dysplasia and HCC[70]
UHRF1 (Human)ConstitutiveAtypical cells, dysplastic foci and HCC[124]
UHRF1 + p53M214 (Human)ConstitutiveAtypical cells, dysplastic foci and HCC[124]
xmrk (Xiphophorus)Tet-on-inducibleHyperplasia, hepatocellular adenoma and HCC[80]
yy1 (Zebrafish)ConstitutiveSteatosis[131]
zfBLP1 (Zebrafish)ConstitutiveHyperplasia[133]
zfMcl-1α (Zebrafish)ConstitutiveHyperplasia[133]