Abstract
Human Elongator complex, which plays a key role in transcript elongation in vitro assay, is incredibly similar in either components or function to its yeast counterpart. However, there are only a few studies focusing on its target gene characterization in vivo. We studied the effect of down-regulation of the human elongation protein 3 (hELP3) on the expression of HSP70 through antisense strategy. Transfecting antisense plasmid p1107 into HeLa cells highly suppressed hELP3 expression, and substantially reduced expression of HSP70 mRNA and protein. Furthermore, chromatin immunoprecipitation assay (ChIP Assay) revealed that hElp3 participates in the transcription elongation of HSPA1A in HeLa cells. Finally, complementation and ChIP Assay in yeast showed that hElp3 can not only complement the growth and slow activation of HSP70 (SSA3) gene transcription, but also directly regulates the transcription of SSA3. On the contrary, these functions are lost when the HAT domain is deleted from hElp3. These data suggest that hElp3 can regulate the transcription of HSP70 gene, and the HAT domain of hElp3 is essential for this function. These findings now provide novel insights and evidence of the functions of hELP3 in human cells. © 2011 Li et al.
Original language | American English |
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Journal | PLoS ONE |
Volume | 6 |
State | Published - Jan 1 2011 |
Keywords
- Base Sequence
- Blotting
- DNA Primers
- Down-Regulation
- ELP3 protein
- Genetic Complementation Test
- HSP70 Heat-Shock Proteins
- HSP70 gene
- HeLa Cells
- HeLa cell
- Histone Acetyltransferases
- Humans
- Messenger
- Nerve Tissue Proteins
- Northern
- Northern blotting
- RNA
- Real-Time Polymerase Chain Reaction
- Western
- Western blotting
- antisense oligonucleotide
- article
- chromatin immunoprecipitation
- controlled study
- down regulation
- elongation factor 3
- enzyme activity
- gene
- gene deletion
- gene expression
- gene expression regulation
- genetic complementation
- genetic transfection
- genetics
- heat shock protein 70
- histone acetyltransferase
- human
- human cell
- messenger RNA
- metabolism
- nerve protein
- nucleotide sequence
- physiology
- plasmid
- primer DNA
- protein domain
- protein function
- real time polymerase chain reaction
- transcription initiation
- transcription regulation
Disciplines
- Genetics