TY - JOUR
T1 - Intramolecular triplex potential sequence within a gene down regulates its expression in vivo
AU - Sarkar, Partha S.
AU - Brahmachari, Samir K.
N1 - Funding Information:
The authors acknowledge Department of Biotechnology (India), for financial support, P.Balagurumoorthy for oligonucleotide synthesis, Dr. P.Burma for valuable suggestions on experimental work, Dr.Vani Brahmachari and R.Bagga for critical comments on the manuscript. PSS is senior research fellow of Council of Scientific and Industrial Research (India).
PY - 1992/11/11
Y1 - 1992/11/11
N2 - Polypurine/polypyrimidine sequences have been shown to adopt intramolecular triple helix structures under torsional stress and/or at low pH. Such sequences have been observed within the the regulatory as well as the coding regions of several genes and the involvement of triple helical structure adopted by these sequences in transcriptional control has heen speculated. Taking advantage of codon degeneracy we have engineered a 38 bp long intramolecular triple helix potential polypurine/polypyrimidine sequence motif between the 37th and 50th codons of β-galactosidase gene in the plasmid pBluescriptllSK + to investigate whether in vivo E.coli RNA polymerase would transcribe sequence motifs adopting triple helix structure, when present within the coding region of the gene. E.coli JM109 cells transformed with this construct pSBT1, exhibited 80% inhibition of β-galactosidase expression compared to another construct pSBmT12 made using less preferred codons for identical amino acid sequence, but lacking the polypurine/polypyrimidine sequence motif. Truncated β-galactosidase transcripts were observed for pSBT1 but not for pSBmT12. Here we report that a putative triple helix potential sequence within a gene can down regulate its expression by partially blocking the transcription elongation in vivo.
AB - Polypurine/polypyrimidine sequences have been shown to adopt intramolecular triple helix structures under torsional stress and/or at low pH. Such sequences have been observed within the the regulatory as well as the coding regions of several genes and the involvement of triple helical structure adopted by these sequences in transcriptional control has heen speculated. Taking advantage of codon degeneracy we have engineered a 38 bp long intramolecular triple helix potential polypurine/polypyrimidine sequence motif between the 37th and 50th codons of β-galactosidase gene in the plasmid pBluescriptllSK + to investigate whether in vivo E.coli RNA polymerase would transcribe sequence motifs adopting triple helix structure, when present within the coding region of the gene. E.coli JM109 cells transformed with this construct pSBT1, exhibited 80% inhibition of β-galactosidase expression compared to another construct pSBmT12 made using less preferred codons for identical amino acid sequence, but lacking the polypurine/polypyrimidine sequence motif. Truncated β-galactosidase transcripts were observed for pSBT1 but not for pSBmT12. Here we report that a putative triple helix potential sequence within a gene can down regulate its expression by partially blocking the transcription elongation in vivo.
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U2 - 10.1093/nar/20.21.5713
DO - 10.1093/nar/20.21.5713
M3 - Article
C2 - 1454535
AN - SCOPUS:0026437556
SN - 0305-1048
VL - 20
SP - 5713
EP - 5718
JO - Nucleic acids research
JF - Nucleic acids research
IS - 21
ER -