HULC was discovered as the first IGF2BP substrate that is not stabilized or translationally regulated, but destabilized by way of CNOT1-mediated deadenylation recruited by IGF2BP1. Sixty human HCCs were analyzed for HULC expression using microarray analysis. Median age at surgery was 57 years (range 16-78), and the male/female ratio was 4:1. All diagnoses were confirmed by histological reevaluation, and use of the samples was approved by the local Ethics Committee.

The cohort contained a balanced repertoire of relevant underlying etiologies: hepatitis B virus (HBV) (n = 15), HCV (n = 12), alcohol (n = 10), cryptogenic (presumably mostly nonalcoholic fatty liver disease [NAFLD]; n = 19) or genetic hemochromatosis Rucaparib molecular weight (n = 3). The patients’ characteristics are

Fulvestrant molecular weight shown in Supporting Table 1. For in vitro transcription, the Megascript T7 kit (Life Technologies, Carlsbad, CA) was used according to the manufacturer’s recommendations. Briefly, 1 μg linearized plasmid template was used and reactions were incubated for 16 hours in the presence or absence of Biotin-16-UTP (Epicentre, Madison, WI). The ratio between UTP and Biotin-16-UTP was 20:1. The reaction was stopped by addition of 1 μL Turbo-DNase. RNA was precipitated with LiCl. RNA integrity and size were controlled using agarose gel electrophoresis. Beads were preblocked with 1 mg/mL BSA (Roche), 0.2 mg/mL yeast tRNA (Roche), and 0.2 mg/mL Glycogen (Carl check details Roth, Karlsruhe, Germany) in low salt wash buffer (20 mM Hepes, pH 7.9; 100 mM KCl; 10 mM MgCl2; 0.01% NP40; 1 mM DTT) before addition of RNA. RNA was incubated with 50 μL Streptavidine-Sepharose beads (GE Healthcare, Little Chalfont, UK) in 500 μL HS-WB300 (20 mM Hepes, pH 7.9; 300 mM KCl; 10 mM MgCl2; 0.01% NP40; 1 mM DTT) for 4 hours. Unbound RNA was washed away with 3× 1 mL HS-WB400 (20 mM Hepes, pH 7.9; 400 mM KCl; 10 mM

MgCl2; 0.01% NP40; 1 mM DTT). Cytoplasmic cell extract (2-3 mg) was added and incubated overnight at 4°C. The next day the extract was removed and beads were washed 6 times with 1 mL HS-WB400. Beads were resuspended in 50 μL 6 M urea; 1 mM DTT; 0.01% NP-40 and incubated at room temperature for 30 minutes in a shaking block at 900 rpm. Then the supernatant was transferred into a new tube and proteins were precipitated with 5 volumes of prechilled acetone for 1 hour at −20°C. Proteins were pelleted by way of centrifugation at 13,000g at room temperature. Pellets were washed twice with 1 mL 80% ethanol, dried for 5 minutes, and resuspended in 20 μL protein sample buffer. HepG2 cells were transfected with small interfering RNAs (siRNAs) as stated above. After 48 hours, alpha-amanitine (AppliChem, Darmstadt, Germany) was added (10 μg/mL f.c.) and cells were harvested at the indicated timepoints. All experiments were done in biological triplicates.