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Protein Synthesis Transcription
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Transcription Initiation Elongation Termination
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Transcription- Initiation
The enzyme, RNA Polymerase, binds to the segment of DNA that is to be transcribed Once, RNA Polymerase binds, it opens the double helix and transcription begins This occurs both in prokaryotes and eukaryotes DNA transcription is not a random phenomenon If RNA polymerase randomly transcribed DNA, the cell would not make the correct polypeptide
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Transcription- Initiation
RNA polymerase binds to the DNA molecule upstream of the gene to be transcribed Upstream: Region of DNA adjacent to the start of a gene The upstream region is a sequence on one strand of DNA located adjacent to the start of the gene
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Upstream Region This region indicates where the RNA polymerase should start transcribing and which DNA strand should be transcribed This upstream region is know as the promoter In most genes, the promoter consists of a characteristic base-pair pattern
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Promoter Promoter region in DNA is high in adenine and thymine bases, which serve as a recognition site for RNA Polymerase A=T share only 2 hydrogen bonds as compared with C and G that share 3 H bonds It takes less energy to break to 2 bonds instead of 3
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Transcription-Elongation
Elongation starts as soon as the RNA Polymerase moves to the start of the gene and binds to the promoter It then opens up the double helix and starts building the single-stranded mRNA in the 5'-3' direction Unlike the case in DNA replication, the RNA polymerase does not require a primer to start building the complementary strand
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Transcription- Elongation
Note: The promoter itself does not get transcribed The process of elongation of the RNA transcript is similar to that of DNA replication RNA uses only one of the strands of DNA as a template for mRNA synthesis This chosen DNA strand is called the template strand The strand not used for transcription is the coding strand
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Know your strands DNA Replication mRNA Transcription
Done by DNA polymerase DNA synthesized in the 5'-3' direction Leading strand: strand synthesized continuously, using the 3'-5' template strand as its guide and is build toward the replication fork Lagging strand: strand synthesized discontinuously in the opposite direction to replication fork mRNA Transcription Done by RNA polymerase mRNA synthesized in the 5'-3' direction Template strand: strand of DNA that RNA polymerase uses as a guide to build complementary mRNA Coding strand: strand of DNA that is not used for transcription and is identical in sequence to mRNA except it contains thymine instead of uracil* (p.242)
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Know your strands Both DNA and mRNA are synthesized in the 5'-3' direction
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Transcription- Termination
mRNA is synthesized until the end of the gene is reached Terminator sequence: RNA Polymerase recognizes the end of the gene when it comes across this sequence Then, the newly synthesized mRNA dissociates with the DNA template strand Transcription stops and RNA Polymerase is free to bind to another promoter region and transcribe another gene
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mRNA Synthesis
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Posttranscriptional Modifications:
In eukaryotes, mRNA cannot leave the nucleus directly following transcription mRNA must be modified to primary transcript A 5' cap is added to the start of the primary transcript
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Structure of the 5' cap 7-methyl guanosine forming a modified guanine nucleoside triphosphate Part of mRNA transcript 5’ end of mRNA transcript
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5' cap Added to the start of primary transcript
Function: protects the mRNA from digestion by enzymes such as nucleases and phosphatases as it exits the nucleus and enters cell cytoplasm Plays a role in initiation of translation
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Further mRNA Modificatin:
Poly-A tail Enzyme poly-A polymerase involved in furhter modification of mRNA Enzyme responsible for adding a string of ~ 200 adenine ribonucleotides to the 3' end of mRNA This string is known as the poly-A tail This is done to protect the mRNA from degradation later on
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Capping and Tailing Addition of a 5' cap and a poly-A tail to the primary transcript is a process known as capping and tailing
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Further Modification DNA of a eukaryotic gene is made of various regions Exons: Segments of DNA that code for part of a specific protein Introns: Non-coding regions of a gene The introns are interspersed among the exons
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Introns and Exons Primary transcript contains both introns and exons, i.e, it contains both regions that code and those that do not code for part of the protein If the introns (non-coding regions) are translated, the protein will not fold properly causing the proteins to be dysfunctional and useless to the cell Therefore, before the primary transcript leaves the nucleus, the introns are removed
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Spliceosomes Particles made of RNA and protein
They cut introns from mRNA primary transcript And join together the remaining coding exon regions mRNA exits the nucleus, but the introns stay, where they get degraded and recycled
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mRNA transcript Primary transcript gets capped
Primary transcript gets tailed The introns get excised Primary transcript transformed to mRNA transcript mRNA transcript exits nucleus into the cytoplasm mRNA transcript ready to be translated by a ribosome into a protein
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mRNA is not error proof Unlike DNA replication, there is no quality control enzyme to ensure that the mRNA transcript is correct Therefore, more errors are made during transcription than translation Errors are not as detrimental as those occurring during DNA replication, since a single gene is transcribed repeatedly to make hundreds of transcripts
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