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B Wani

Publications and source records attributed to B Wani.

2 recordsLinked to original sources

The Ski oncoprotein interacts with Skip, the human homolog of Drosophila Bx42.

The v-Ski avian retroviral oncogene is postulated to act as a transcription factor. Since protein-protein interactions have been shown to play an important role in the transcription process, we attempted to identify Ski protein partners with the yeast two-hybrid system. Using v-Ski sequence as bait, the human gene skip (Ski Interacting Protein) was identified as encoding a protein which interacts with both the cellular and viral forms of Ski in the two-hybrid system. Skip is highly homologous to the Drosophila melanogaster protein Bx42 which is found associated with chromatin in transcriptionally active puffs of salivary glands. The Ski-Skip interaction is potentially important in Ski's transforming activity since Skip was demonstrated to interact with a highly conserved region of Ski required for transforming activity. Like Ski, Skip is expressed in multiple tissue types and is localized to the cell nucleus.

Amino Acid Sequence↗

Does magnesium modify left ventricular remodeling after experimental myocardial infarction?

BACKGROUND: Magnesium therapy has been shown to improve survival and decrease the incidence of left ventricular failure when given to patients shortly after a myocardial infarction, but the mechanisms are unknown. We tested the hypothesis that the benefits of magnesium therapy are due to a favorable effect on early left ventricular remodeling, particularly on infarct shape changes. METHODS: Rats were infarcted and randomly allocated to two groups: group 1 (n = 8) received intravenous magnesium sulfate (200 mumol/kg) over 10 min started 30 min after coronary ligation, then an intraperitoneal dose (800 mumol/kg), which was repeated 6 h later. Group 2 (n = 10) served as a control group, and received normal saline. Using this regimen, the trough level of ionized magnesium 12 h after the intravenous dose was 33% above the control level. Three weeks after infarction, the hearts of the rats were arrested with saturated potassium chloride and fixed in formalin at 7.5 mmHg. The hearts were cut transversely into four slices. Photographs of both sides of each slice were taken and projected for morphometric analysis. RESULTS: Infarct size was similar in the magnesium and control groups (35 +/- 4 versus 30 +/- 2%). Infarct thickness, expansion index, and cavity area were also similar in both groups. CONCLUSIONS: Magnesium has no effect on early left ventricular remodeling or infarct expansion. The mechanism of its clinical benefits remains unexplained.

Animals↗