Nucleic acid metabolism encompasses the synthesis and degradation of nucleic acids, which include DNA and RNA. These processes are vital for the maintenance, replication, and expression of genetic information.
 DNA Metabolism
1. DNA Replication:
– Initiation: Replication begins at specific locations in the genome called origins of replication. Initiator proteins bind to these origins, causing the DNA to unwind and form a replication bubble.
– Elongation: DNA polymerase synthesizes the new DNA strand by adding nucleotides complementary to the template strand. This process occurs in a 5’ to 3’ direction.
– Leading and Lagging Strands: The leading strand is synthesized continuously, while the lagging strand is synthesized in short segments called Okazaki fragments, which are later joined by DNA ligase.
– Proofreading and Repair: DNA polymerase has proofreading activity to correct errors. Additional repair mechanisms, such as mismatch repair and excision repair, help maintain DNA integrity.
2. DNA Repair:
– Base Excision Repair (BER): Repairs small, non-helix-distorting base lesions. DNA glycosylases remove damaged bases, and the resulting abasic site is processed by endonucleases and polymerases.
– Nucleotide Excision Repair (NER): Repairs bulky, helix-distorting lesions. A segment of the DNA strand containing the damage is removed and replaced.
– Mismatch Repair (MMR): Corrects errors introduced during DNA replication that escape proofreading.
3. DNA Recombination:
– Homologous Recombination: Involves the exchange of genetic material between homologous DNA molecules. This process is critical during meiosis for genetic diversity.
– Non-Homologous End Joining (NHEJ): Repairs double-strand breaks by directly ligating the broken ends, often leading to mutations.
 RNA Metabolism
1. Transcription:
– Initiation: RNA polymerase binds to a promoter region on the DNA and unwinds the DNA strands.
– Elongation: RNA polymerase moves along the DNA template strand, synthesizing RNA in the 5’ to 3’ direction.
– Termination: RNA polymerase reaches a termination sequence, causing the release of the newly synthesized RNA.
2. RNA Processing:
– Capping: Addition of a 7-methylguanosine cap to the 5’ end of pre-mRNA, which protects the RNA from degradation and assists in ribosome binding.
– Splicing: Removal of non-coding introns and joining of exons. This process is carried out by the spliceosome.
– Polyadenylation: Addition of a poly(A) tail to the 3’ end of pre-mRNA, which enhances stability and facilitates export to the cytoplasm.
3. RNA Degradation:
– RNA molecules are degraded by exonucleases and endonucleases. This process is crucial for regulating gene expression and RNA quality control.
Genetic Information Transfer
The transfer of genetic information involves several key processes: replication, transcription, and translation. Together, these processes allow the flow of genetic information from DNA to RNA to protein, often referred to as the central dogma of molecular biology.
Replication
– Purpose: To accurately copy the entire genome before cell division.
– Enzymes Involved: DNA polymerase, helicase, primase, ligase, and topoisomerase.
Transcription
– Purpose: To synthesize RNA from a DNA template.
– Enzymes and Factors Involved: RNA polymerase, transcription factors, and RNA processing enzymes.
Translation
– Purpose: To synthesize proteins using the mRNA template.
– Key Steps:
– Initiation: The ribosome assembles around the mRNA, and the first tRNA binds to the start codon.
– Elongation: tRNAs bring amino acids to the ribosome, matching their anticodons to the mRNA codons, and the ribosome catalyzes peptide bond formation.
– Termination: The ribosome reaches a stop codon, releasing the completed polypeptide.
– Molecules Involved: Ribosomes, mRNA, tRNA, amino acids, and various initiation, elongation, and release factors.
Regulation of Genetic Information Transfer
1. Transcriptional Regulation:
– Promoters and Enhancers: DNA sequences that regulate the binding of RNA polymerase and transcription factors.
– Transcription Factors: Proteins that bind to specific DNA sequences to activate or repress transcription.
– Epigenetic Modifications: DNA methylation and histone modifications that influence gene expression without altering the DNA sequence.
2. Post-Transcriptional Regulation:
– Alternative Splicing: Produces different mRNA variants from the same gene.
– mRNA Stability: Controlled by RNA-binding proteins and microRNAs that can promote or inhibit mRNA degradation.
3. Translational Regulation:
– Initiation Factors: Proteins that regulate the assembly of the ribosome on the mRNA.
– mRNA Localization: mRNAs can be transported to specific cellular locations for localized protein synthesis.
4. Post-Translational Regulation:
– Protein Modifications: Phosphorylation, acetylation, ubiquitination, and other modifications that affect protein activity, stability, and interactions.
– Protein Degradation: Proteins can be targeted for degradation by the ubiquitin-proteasome system.
Summary
Nucleic acid metabolism and genetic information transfer are fundamental processes that ensure the accurate replication, expression, and regulation of genetic information. These processes involve a complex interplay of enzymes, regulatory factors, and cellular machinery, working together to maintain the integrity and functionality of the genome. Understanding these processes is crucial for insights into cellular function, development, and disease mechanisms.
