Track template direction and processed transcript length
Transcription makes RNA complementary to a DNA template read 3′→5′, with RNA extended 5′→3′. The coding strand, written in the same 5′→3′ orientation as the RNA, matches its sequence except DNA T corresponds to RNA U. A promoter helps define initiation and which strand is used for a particular gene; neither strand is the universal template for an entire chromosome.
Learning outcome: Compare exon retention and skipping with the same tail, then vary tail without changing exon choice. Keep primary RNA, mature RNA, coding length and residue count separate. Independently derive the short template example with both end labels.
Starting recap
Trace strand direction, processing and molecular accounting; distinguish synthesis from abundance, local from shared regulation, and conditional assay evidence from identity or function claims.
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Try
The primary transcript is 500 nt. Retaining all exons gives 360 nt before the tail; a 40 nt tail gives 400 nt by the stated convention. Coding length including stop is 360−30−27=303 nt, encoding (303−3)/3=100 residues. Skipping the 90 nt exon gives 70 residues, not a frameshift in this packet.
Open the experimentPredict
Does adding 60 nt to a poly(A) tail add 20 amino acids to the protein?
Experiment
Compare exon retention and skipping with the same tail, then vary tail without changing exon choice. Keep primary RNA, mature RNA, coding length and residue count separate. Independently derive the short template example with both end labels.
Separate transcribed length, exon retention and protein coding
Worked teaching model · synthetic values · Original transcript has exons120,90,150 nt and introns80,60 nt. First exon contains30 nt 5′UTR; last contains27 nt 3′UTR and a3 nt stop codon. Middle exon is in-frame90 nt. Length accounting excludes the added cap nucleotide; supplied poly(A) tail is not translated.
Reset keeps your prediction, captures and practice history.
RNA length, coding length and peptide length differ because UTRs, tail and stop are not amino-acid codons.
The supplied in-frame exon skip removes30 residues without shifting the remaining frame. A cap and poly(A) tail support processing/stability/export but are not simply translated extension sequences. Exons can include untranslated regions.
| Quantity | Value | Unit |
|---|---|---|
| Primary transcript length | 500 | nt |
| Retained exon length | 360 | nt |
| Mature RNA length including supplied tail | 400 | nt |
| Coding region including stop | 303 | nt |
| Encoded amino-acid residues | 100 | residues |
| Introns removed | 140 | nt |
| Skipped exon removed | 0 | nt |
Retain prior predictions, settings and quantities in the notebook. These are original supplied/calculated comparisons, not physical specimen observations or laboratory participation.
RNA length, coding length and peptide length differ because UTRs, tail and stop are not amino-acid codons.
The supplied in-frame exon skip removes30 residues without shifting the remaining frame. A cap and poly(A) tail support processing/stability/export but are not simply translated extension sequences. Exons can include untranslated regions.
Captures preserve recipes and replay their calculated results. They are synthetic model evidence, not physical measurements.
Understand
Apply
Public practice checks a specific claim. It does not establish independent mastery.
A processed transcript has 420 retained exon nucleotides, 45 nt 5′UTR, 42 nt 3′UTR and one stop codon. It receives an 80 nt tail. Find mature length by the stated cap-excluding convention and encoded residues.
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