Slide 1

Molecular Basis of Inheritance - Termination of Protein Synthesis

• The process of protein synthesis involves three main steps: initiation, elongation, and termination.
• Termination of protein synthesis occurs when the ribosome encounters a stop codon on the mRNA.
• Stop codons include UAG, UAA, and UGA.
• When a stop codon is encountered, a release factor protein binds to the ribosome, causing the release of the completed protein chain.

Slide 2

Termination Codons and Release Factors

• Stop codons signal the termination of protein synthesis.
• Release factors are proteins that recognize and bind to stop codons.
• Release factor 1 (RF1) recognizes UAA and UAG stop codons.
• Release factor 2 (RF2) recognizes UAA and UGA stop codons.
• Release factor 3 (RF3) helps in the termination process by promoting the dissociation of the ribosome from the mRNA.

Slide 3

Peptide Release and Ribosome Recycling

• During termination, the growing polypeptide chain is released from the ribosome.
• The release factors catalyze the hydrolysis of the bond between the polypeptide chain and the tRNA in the P-site.
• This results in the release of the completed protein.
• The ribosome then dissociates into its subunits, ready to start a new round of translation.

Slide 4

Termination in Eukaryotes

• Termination of protein synthesis in eukaryotes is slightly different from that in prokaryotes.
• Eukaryotes have a release factor called eRF1 that recognizes all three stop codons.
• eRF1 binds to the ribosome and triggers the release of the completed protein.
• The ribosome then disassembles, and the subunits are recycled.

Slide 5

Termination and the Poly(A) Tail

• In eukaryotes, the presence of a poly(A) tail on the mRNA plays a role in termination.
• The poly(A) tail interacts with poly(A)-binding proteins (PABPs) and release factors such as eRF3.
• These interactions help in the termination process and facilitate the release of the completed protein.

Slide 6

Termination and Ribosomal Recycling

• After termination, ribosomes need to be recycled for the next round of translation.
• The recycling process involves the release of the mRNA, tRNAs, and release factors from the ribosome.
• The ribosome subunits dissociate and are ready to bind to a new mRNA molecule and initiate translation.

Slide 7

Factors Influencing Termination Efficiency

• Several factors can influence the efficiency of termination.
• The sequence context surrounding the stop codon can affect the rate of termination.
• The presence of certain RNA secondary structures can also impact termination efficiency.
• The availability of release factors and other termination proteins can influence the efficiency of termination.

Slide 8

Termination and Polypeptide Folding

• Termination is crucial for proper polypeptide folding.
• If termination is incomplete or incorrect, it can lead to misfolded proteins.
• Misfolded proteins can have detrimental effects on cellular processes and may contribute to diseases such as Alzheimer’s and Parkinson’s.

Slide 9

Termination Mutations

• Mutations in the genes encoding release factors or other termination proteins can lead to termination defects.
• These mutations can affect the efficiency of termination or cause premature termination.
• Defects in termination can have severe consequences and are associated with various genetic disorders.

Slide 10

Conclusion

• Termination is the final step in protein synthesis, involving the recognition of stop codons and the release of the completed protein.
• Release factors play a crucial role in the termination process.
• Termination differs slightly between prokaryotes and eukaryotes.
• Proper termination is essential for correct polypeptide folding and cellular function.

Slide 11

Termination Signals

• Termination signals are encoded by specific DNA sequences that mark the end of a gene.
• The most common termination signal is a DNA sequence called a terminator or polyadenylation signal.
• Depending on the organism, terminators can vary in length and sequence.

Slide 12

Polyadenylation signal

• The polyadenylation signal consists of a sequence of DNA nucleotides that direct the addition of a poly(A) tail to the mRNA.
• The poly(A) tail plays a role in the stability and translation efficiency of the mRNA molecule.
• In eukaryotes, the polyadenylation signal is usually located downstream of the coding region.

Slide 13

Transcription Termination in Bacteria

• Transcription termination in bacteria is mediated by two major mechanisms: Rho-dependent termination and Rho-independent termination.
• Rho-dependent termination involves the protein Rho, which binds to a specific sequence in the mRNA called the Rho utilization (rut) site.
• Rho moves along the mRNA molecule, destabilizing the RNA-DNA hybrid and causing termination.

Slide 14

Rho-Independent Termination

• Rho-independent termination, also known as intrinsic termination, relies on a specific DNA sequence in the mRNA called the terminator.
• The terminator sequence consists of an inverted repeat followed by a string of adenine nucleotides.
• When the RNA polymerase reaches the terminator, a hairpin structure forms in the mRNA, causing the RNA polymerase to pause and eventually dissociate.

Slide 15

Termination in Eukaryotes

• Transcription termination in eukaryotes is more complex than in bacteria.
• It involves the recognition and processing of the polyadenylation signal.
• After the mRNA is transcribed, multiple proteins bind to the polyadenylation signal and cleave the nascent mRNA.
• The cleaved mRNA is then polyadenylated, resulting in the addition of a poly(A) tail.

Slide 16

Termination Factors in Eukaryotes

• Several proteins are involved in the termination process in eukaryotes.
• The cleavage and polyadenylation specificity factor (CPSF) recognizes and binds to the polyadenylation signal.
• The cleavage stimulation factor (CstF) stimulates the cleavage of the mRNA.
• Other proteins, such as poly(A) polymerase (PAP) and poly(A) binding protein (PABP), are also involved in polyadenylation.

Slide 17

Regulation of Termination

• Termination can be regulated to control gene expression.
• In bacteria, the presence of certain sequences or proteins can affect the efficiency of termination.
• In eukaryotes, specific DNA sequences and factors can influence the choice of polyadenylation site, resulting in alternative polyadenylation.

Slide 18

Termination and Gene Regulation

• Proper termination is essential for gene regulation.
• Incorrect termination can lead to read-through transcription, where the RNA polymerase continues transcribing downstream genes.
• This can result in aberrant gene expression and disruption of normal cellular processes.

Slide 19

Applications and Research

• Understanding the mechanisms of transcription termination has many applications.
• It can help in the development of new therapeutic strategies for diseases related to misregulated gene expression.
• Researchers are also studying how termination factors and processes contribute to genetic disorders and cancer.

Slide 20

Summary

• Termination signals mark the end of a gene and are important for proper gene expression.
• In bacteria, termination can be mediated by the protein Rho or occur independently.
• In eukaryotes, termination involves the recognition and processing of the polyadenylation signal.
• Termination is regulated to control gene expression and prevent read-through transcription.
• Research in termination mechanisms has broad applications in medicine and genetics.

Slide 21

Factors Influencing Termination Efficiency (cont’d)

• RNA secondary structures, such as hairpins, can slow down or hinder termination.
• The presence of certain proteins, such as NusA in bacteria, can affect termination efficiency.
• The speed of RNA polymerase during transcription can also influence termination efficiency.
• The availability of nucleotides and other factors required for termination can impact efficiency.

Slide 22

Termination and Antibiotics

• Some antibiotics target the termination process in bacteria.
• For example, spectinomycin and hygromycin B interfere with the binding of tRNA to the ribosome during termination.
• Streptogramin antibiotics inhibit release factor function, preventing termination.
• Understanding termination is crucial for the development of new antibiotics and combating antibiotic resistance.

Slide 23

Termination and Gene Editing

• Termination signals are essential for precise gene editing using techniques like CRISPR-Cas9.
• By targeting termination signals, researchers can disrupt gene expression or introduce specific changes in the DNA sequence.
• This has significant implications for genetic research, therapeutics, and potential treatment of genetic disorders.

Slide 24

Termination and Gene Expression Regulation

• Efficient termination is important for proper regulation of gene expression.
• Termination signals help determine the boundaries of genes and ensure accurate transcript termination.
• Variations in termination efficiency can contribute to gene expression changes and phenotypic diversity.

Slide 25

Termination and Disease

• Abnormal termination can lead to the production of truncated or abnormal proteins.
• This can result in various genetic disorders, including certain subtypes of muscular dystrophy and neurodegenerative diseases.
• Understanding the factors that affect termination can help in developing therapeutic strategies for these diseases.

Slide 26

Termination and DNA Replication

• Termination of DNA replication is a separate process from transcription termination.
• Termination sequences in DNA regulate the unwinding and separation of replicated DNA strands.
• Failure of DNA replication termination can lead to genomic instability and chromosomal aberrations.

Slide 27

Termination Signals in Eukaryotic Genes

• In eukaryotes, termination signals differ from those in prokaryotes.
• Eukaryotic genes often have multiple termination sites, allowing for alternative splicing and regulation of gene expression.
• Termination signals in eukaryotes can include specific RNA sequences and signals recognized by termination factors.

Slide 28

Alternative Polyadenylation and Termination

• Alternative polyadenylation is a process that generates multiple mRNA isoforms from a single gene.
• It involves the use of different polyadenylation sites within the gene.
• Termination signals play a crucial role in determining which polyadenylation site is used and which mRNA isoform is produced.

Slide 29

Termination in Viral Genomes

• Viral genomes also utilize termination signals for proper gene expression.
• The termination of viral gene transcription is influenced by specific sequences and viral termination factors.
• The understanding of viral termination mechanisms is essential for developing antiviral therapeutics.

Slide 30

Conclusion

• Termination of protein synthesis and transcription is a fundamental process in molecular biology.
• Termination signals and factors play critical roles in ensuring accurate gene expression and protein synthesis.
• Termination efficiency can be influenced by various factors, such as sequence context, RNA secondary structures, and the availability of termination factors.
• Abnormal termination can have significant consequences, leading to genetic disorders and disease.
• Research on termination mechanisms has broad implications for medicine, understanding genetic disorders, and developing therapeutic strategies.