Most of Your DNA Does Not Code for Polypeptides, Yet It Is Far From JunkMost of the genome is non-coding DNA, meaning it is not translated into polypeptides.These sequences still carry out essential functions in gene expression, chromosome stability, and protein synthesis.Calling them "junk DNA" is misleading, because losing them would disrupt how cells build and control proteins.NoteNon-coding DNA is any region of the genome that is not translated into a polypeptide.It includes regulators of gene expression, introns, telomeres, and the genes for rRNA and tRNA.Regulatory Sequences Control When and How Strongly Genes Are ExpressedRegulatory sequences are non-coding DNA that switch genes on or off and tune their output.PromotersThese are the sites where RNA polymerase binds to begin transcription.EnhancersThese distant sequences increase transcription of a gene.SilencersThese sequences decrease or shut down transcription of a gene.NoteHow promoters and enhancers drive transcription initiation is covered in detail in D1.2.13.Regulatory sequences are often highly conserved across species, which signals their importance.Introns Are Removed From mRNA but Still Shape Gene FunctionIntrons are non-coding sequences within a gene that are removed during RNA processing.The remaining coding sequences, the exons, are joined together to form the mature mRNA.Alternative splicingBecause introns separate the exons, exons can be joined in different combinations so one gene can produce several polypeptides.RegulationSome introns contain enhancers or silencers that influence gene expression.Evolutionary flexibilityMutations can accumulate in introns without changing the coding sequence, giving genes room to evolve.NoteThe detailed mechanism of alternative splicing is covered in D1.2.16, so here you only need to know that introns make it possible.Telomeres Cap Chromosome Ends and Limit How Often a Cell Can DivideTelomeres are repetitive non-coding sequences at the ends of chromosomes.They stop chromosomes from fraying or sticking to one another.Telomeres shorten a little with each round of DNA replication.Once they become too short, the cell can enter senescence or undergo programmed cell death, which limits further division.Cancer cells often reactivate the enzyme telomerase to rebuild their telomeres and keep dividing indefinitely.AnalogyTelomeres work like the plastic tips on shoelaces.They take the wear of replication so the coding DNA underneath stays intact.Genes for rRNA and tRNA Build the Machinery of TranslationSome non-coding genes are transcribed into functional RNA rather than being translated into a polypeptide.The genes for rRNA and tRNA are examples, because their end product is the RNA molecule itself.Ribosomal RNA (rRNA)rRNA forms the core of ribosomes, the structures that assemble polypeptides.It catalyses the formation of peptide bonds, making it a ribozyme, an RNA with enzyme activity.Transfer RNA (tRNA)Each tRNA carries a specific amino acid and has an anticodon that pairs with a matching mRNA codon.This pairing ensures the correct amino acid is added to the growing polypeptide.ExampleThe mRNA codon AUG pairs with the anticodon UAC on a tRNA carrying methionine, the start amino acid for most proteins.Active recallName four types of non-coding DNA sequence that have a function.What is the difference between an enhancer and a silencer?Why does the presence of introns allow one gene to produce several polypeptides?What happens to a cell when its telomeres become too short, and how do cancer cells avoid this?What role does rRNA play in the ribosome, and why is it called a ribozyme?