IRESite record type: plasmid_with_promoter_and_putative_IRES_translationally_characterized
The shape of the nucleic acid molecule translated: linear
The quality of the mRNA/+RNA sequence: our_best_guess
The mRNA/+RNA description:
Putative spliced in vivo transcript of pR-deltaEMCV-F with 101-1 insert of putative LINE-1 IRES from SV40
promoter
The mRNA/+RNA sequence represented in the +DNA notation:
Warning: mRNA sequence when devoid of trailing 'A's is still not a substring of the plasmid sequence. Is it because an intron is spliced out? Stay calm then. :-)
Credibility of mRNA sequence: end-to-end_sequence_reverse_engineered_and_should_match_experiment
The name of the promoter used to express this mRNA: SV40
The in vivo produced transcripts are heterogeneous (due to any of promoter?/splicing?/cleavage?/breakage?): not tested
The in vivo produced heterogeneous transcripts occur due to alternative splicing: not tested
A promoter reported in cDNA corresponding to IRES sequence: no
Summary of possible issues when IRES cDNA is experimentally transcribed in vivo:
Summary of experiments studying integrity of the in vivo transcripts in a particular host:
Integrity (uniformity) of mRNA tested using Northern-blot: not_tested
Integrity (uniformity) of mRNA tested using RNase protection: not_tested
Integrity (uniformity) of mRNA tested using 5'-RACE: not_tested
Integrity (uniformity) of mRNA tested using primer extension : not_tested
Integrity (uniformity) of mRNA tested using RT-PCR: not_tested
Integrity (uniformity) of mRNA tested using real-time quantitative polymerase chain reaction (rtqPCR): not_tested
Integrity (uniformity) of mRNA tested using RNAi: not_tested
Integrity (uniformity) of mRNA tested using S1 nuclease mapping: not_tested
Cryptic promoter presence was confirmed by expression from a promoter-less plasmid: no_promoter_confirmed
Cryptic promoter presence was confirmed in an experimental setup involving inducible promoter: not_tested
Integrity (uniformity) of mRNA molecules or possible promoter presence expressed in vivo was tested using another method, please specify in Remarks: not_tested
The description of the protein encoded in this ORF: Firefly luciferase
The translational frameshift (ribosome slippage) involved: 0
The ribosome read-through involved: no
The alternative forms of this protein occur by the alternative initiation of translation: not tested
The ORF absolute position (the base range includes START and STOP codons or their equivalents): 1751-3403
Remarks:
In preparing for submission of this IRESite record, it was found that there are 3 PCR errors (A->G @ 1481,
C->T @ 1649, del @ 1784) and a nucleotide difference between the PCR template and the GenBank database (T->G @
1592).
Overview of the mutants shown in 7B:
mL1-ORF2-138-1-mut1
2804-2941
This tested sequence is identical to "mL1-ORF2-138-1" except for 3 single point mutations [2820(G->C),
2836(A->C), 2838(G->C)] introduced to disrupt a predicted stem-loop.
mL1-ORF2-138-1-mut2
2804-2941
This tested sequence is identical to "mL1-ORF2-138-1" except for 6 single point mutations [2812(C-G),
2815(T-G), 2820(G-C), 2833(C-G), 2836(A-C), 2838(G-C)] introduced to disrupt and then restore a predicted
stem-loop.
mL1-ORF2-138-1-mut32804-2941
This tested sequence is identical to "mL1-ORF2-138-1" except for 5 single point mutations [2810(A-T),
2820(G-C), 2836(A-C), 2838(G-C), 2840(T-A)] introduced to disrupt a predicted stem-loop and avoid introducing
a small ORF.
mL1-ORF2-138-1-mut4
2804-2941
This tested sequence is identical to "mL1-ORF2-138-1" except for 8 single point mutations [2810(A-T),
2812(C-G), 2815(T-G), 2820(G-C), 2833(C-G), 2836(A-C), 2838(G-C), 2840(T-A)] introduced to disrupt/restore a
predicted stem-loop and avoid introducing a small ORF.