The Takeaway: You could be forgiven for confusing the terms “transcription” and “translation.” Not only do they sound similar, but their functions have a degree of similarity to them. Throw replication into the mix and there is even more opportunity for confusion. Despite the similarities, these functions are distinct and worthy of deeper investigation.
All of the cells in a multicellular organism contain the exact same DNA. Despite that, cells containing the same DNA can have profound physiological differences. This occurs because of differential gene expression, a term that refers to the combination of genes that are expressed or repressed in particular cells, making that cell unique.
All of the cells in a multicellular organism contain the exact same DNA. Despite that, cells containing the same DNA can have profound physiological differences. This occurs because of differential gene expression, a term that refers to the combination of genes that are expressed or repressed in particular cells, making that cell unique.
Transcription is the synthesis of RNA from a DNA template. The code in the DNA is converted to a complementary code of RNA.
Translation is the synthesis of a protein from an RNA template. The code of mRNA is converted into a protein’s amino acid sequence.
Replication is what happens when a cell divides and its two strands of DNA split into two single strands, each of which acts as a template for a new strand of complementary DNA.
While DNA replication is an essential cellular process, it is not without its potential problems. Some include:
Transcription is the first step in gene expression. It has three steps:
In eukaryotes, there is a modification step after the polymerase has finished transcribing pre-mRNA. These modifications include the addition of a 5’ cap at the start of the pre-mRNA sequence and a poly-A tail (multiple adenosine monophosphate molecules) at the 3’ end. Splicing is another common RNA modification step in eukaryotes. In prokaryotes RNA modification is not needed, and the transcribed mRNA can be directly translated.
Translation has the same three steps as transcription, though the activities in each are different.
IDT has tools for gene expression using qPCR. qPCR is performed as a one-step or two-step process. One‑step qPCR requires converting the RNA into DNA and measuring the resulting cDNA concentration—this is done in a single tube. Two‑step qPCR also requires the RNA to be reverse transcribed into cDNA, using a reverse transcriptase, but then the cDNA is transferred into a separate tube for a subsequent qPCR reaction.
IDT has a selection of qPCR reagents for gene expression analysis. Choices include easy-to-use PrimeTime™ qPCR Assays, or you can design your own custom assay. Both probe-based and intercalating-dye-based options are available.
Want to learn more about qPCR assay design? IDT’s real-time qPCR guide covers every aspect of probe-based qPCR assays and includes troubleshooting, assay design, data interpretation, and more. Download it here.
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