Abstract
Objective: To clone the full-length cDNA sequence of novel UCA1 spliced isoforms for understanding the exact mechanism of this type of alternative splicing. Methods: The full-length cDNA was amplified from BLZ-211 cells by using the in silicon sequence elongation technique, 5'-RACE and 3'-RACE techniques. Products of RT-PCR were sequenced and further assembled. Results: The new UCA1 spliced isoform sequence was 2202 bp. Conclusion: A combination of the in silicon sequence elongation, 5'-RACE and 3'-RACE techniques is an effective way to obtain the full-length cDNA, which will guide further research on the mechanism of this type of alternative splicing.
| Original language | English |
|---|---|
| Pages (from-to) | 11-13+28 |
| Journal | Journal of Xi'an Jiaotong University (Medical Sciences) |
| Volume | 33 |
| Issue number | 1 |
| State | Published - Jan 2012 |
Keywords
- In silicon
- Rapid amplification of cDNA ends (RACE)
- UCA1