🐇Honors Biology Unit 8 – Gene Expression and Regulation
Gene expression is the process of turning DNA instructions into functional products like proteins. This complex journey involves transcription, where DNA is copied into RNA, and translation, where RNA is decoded to build proteins.
Regulation of gene expression allows cells to adapt to changing conditions and maintain balance. Various mechanisms control when and how genes are expressed, including transcription factors, epigenetic modifications, and post-transcriptional processes.
Gene expression process by which genetic information encoded in DNA is converted into functional products (proteins or RNA)
Transcription synthesis of RNA from a DNA template catalyzed by RNA polymerase
Occurs in the nucleus of eukaryotic cells and cytoplasm of prokaryotic cells
Translation process of decoding mRNA to synthesize polypeptide chains that fold into functional proteins
Genetic code set of rules that specify the correspondence between codons (triplets of nucleotides) and amino acids
Promoter region of DNA located upstream of a gene that initiates transcription and determines where RNA polymerase binds
Enhancers regulatory sequences that can increase the transcription rate of genes
Silencers regulatory sequences that can decrease or suppress the transcription rate of genes
DNA Structure and Function
DNA (deoxyribonucleic acid) double-stranded helical molecule that carries genetic information
Consists of nucleotide monomers each containing a phosphate group, sugar (deoxyribose), and nitrogenous base (adenine, thymine, guanine, or cytosine)
Complementary base pairing adenine pairs with thymine and guanine pairs with cytosine through hydrogen bonds
Antiparallel structure two strands run in opposite directions (5' to 3' and 3' to 5')
DNA packaging in eukaryotes, DNA is tightly coiled around histone proteins to form chromatin, which further condenses into chromosomes
Allows large amounts of DNA to fit inside the nucleus
DNA replication process of making an identical copy of DNA before cell division
Ensures genetic information is passed on to daughter cells
Transcription Process
Transcription first step of gene expression where DNA is used as a template to synthesize complementary RNA
RNA polymerase enzyme responsible for catalyzing the synthesis of RNA from a DNA template
Initiation RNA polymerase binds to the promoter region and unwinds the DNA double helix
Elongation RNA polymerase moves along the DNA template strand (3' to 5') and synthesizes the complementary RNA strand (5' to 3')
Ribonucleotides (ATP, UTP, GTP, and CTP) are added to the growing RNA chain
Termination transcription ends when RNA polymerase reaches a termination sequence, and the newly synthesized RNA is released
Post-transcriptional modifications in eukaryotes, the primary transcript (pre-mRNA) undergoes modifications before becoming mature mRNA
Capping addition of a 7-methylguanosine cap to the 5' end, which protects the mRNA and facilitates translation
Polyadenylation addition of a poly(A) tail (multiple adenine nucleotides) to the 3' end, which stabilizes the mRNA
Splicing removal of non-coding sequences (introns) and joining of coding sequences (exons) to form the final mRNA
Translation and Protein Synthesis
Translation process of decoding the genetic information in mRNA to synthesize polypeptide chains
Ribosomes molecular machines that catalyze the synthesis of proteins by translating mRNA
Consist of two subunits (large and small) composed of ribosomal RNA (rRNA) and proteins
tRNA (transfer RNA) adapter molecules that carry specific amino acids and have anticodons complementary to mRNA codons
Genetic code set of rules that specify the correspondence between codons (triplets of nucleotides) and amino acids
64 possible codons, 61 of which code for amino acids and 3 are stop codons (UAA, UAG, UGA)
Initiation translation begins when the small ribosomal subunit binds to the start codon (AUG) on the mRNA with the help of initiation factors
Elongation tRNA molecules bring amino acids to the ribosome, which are joined together by peptide bonds according to the mRNA sequence
Ribosome moves along the mRNA one codon at a time, adding amino acids to the growing polypeptide chain
Termination translation ends when the ribosome reaches a stop codon (UAA, UAG, or UGA), and the polypeptide chain is released
Post-translational modifications newly synthesized polypeptide chains may undergo modifications (folding, cleavage, addition of functional groups) to form the final functional protein
Gene Regulation Mechanisms
Gene regulation control of gene expression that allows cells to respond to environmental changes and maintain homeostasis
Transcriptional regulation control of gene expression at the level of transcription
Involves transcription factors that bind to regulatory sequences (promoters, enhancers, silencers) and influence RNA polymerase activity
Post-transcriptional regulation control of gene expression after transcription but before translation
Includes mRNA processing (capping, polyadenylation, splicing), mRNA stability, and mRNA transport
Translational regulation control of gene expression at the level of translation
Involves factors that influence ribosome binding, translation initiation, and translation efficiency
Post-translational regulation control of gene expression after translation
Includes protein modifications (phosphorylation, glycosylation, ubiquitination) and protein degradation
Feedback loops regulatory mechanisms that allow cells to maintain stable levels of gene products
Negative feedback loops decrease gene expression when the product accumulates, while positive feedback loops increase gene expression
Epigenetics and Gene Expression
Epigenetics study of heritable changes in gene expression that do not involve alterations to the DNA sequence
DNA methylation addition of methyl groups to cytosine bases, which can silence gene expression
Occurs predominantly at CpG dinucleotides and is catalyzed by DNA methyltransferases (DNMTs)
Histone modifications post-translational modifications of histone proteins (acetylation, methylation, phosphorylation) that can influence chromatin structure and gene expression
Histone acetyltransferases (HATs) add acetyl groups, while histone deacetylases (HDACs) remove them
Histone methyltransferases (HMTs) add methyl groups, while histone demethylases (HDMs) remove them
Chromatin remodeling dynamic changes in chromatin structure that can expose or conceal regulatory sequences and influence gene expression
ATP-dependent chromatin remodeling complexes (SWI/SNF) can slide or evict nucleosomes to alter chromatin accessibility
Epigenetic inheritance transmission of epigenetic marks across generations, which can influence gene expression patterns in offspring
Examples include genomic imprinting (parent-of-origin-specific gene expression) and transgenerational epigenetic inheritance
Genetic Mutations and Their Effects
Mutations changes in the DNA sequence that can alter gene function and expression
Point mutations single nucleotide changes that can be substitutions (one base replaced by another), insertions (extra base added), or deletions (base removed)
Silent mutations do not change the amino acid sequence due to the redundancy of the genetic code
Missense mutations change one amino acid to another, which may or may not affect protein function
Nonsense mutations introduce a premature stop codon, leading to truncated proteins
Frameshift mutations insertions or deletions that shift the reading frame, altering the amino acid sequence and often introducing premature stop codons
Chromosomal mutations large-scale changes in chromosome structure or number
Deletions loss of a chromosomal segment
Duplications extra copies of a chromosomal segment
Inversions reversal of a chromosomal segment
Translocations exchange of chromosomal segments between non-homologous chromosomes
Mutagens factors that can increase the rate of mutations (UV radiation, chemicals, viruses)
DNA repair mechanisms cellular processes that detect and correct DNA damage and mutations
Examples include base excision repair, nucleotide excision repair, and mismatch repair
Real-World Applications and Research
Genetic engineering deliberate modification of an organism's genome using biotechnology techniques
Recombinant DNA technology insertion of foreign DNA into a host organism to produce desired proteins (insulin, growth hormone)
CRISPR-Cas9 gene editing tool that allows precise editing of DNA sequences by creating targeted double-strand breaks
Gene therapy treatment of genetic disorders by introducing functional copies of genes into cells
Ex vivo gene therapy cells are removed, modified, and returned to the patient
In vivo gene therapy genes are directly delivered to target tissues using viral vectors or nanoparticles
Personalized medicine tailoring medical treatments to an individual's genetic profile to optimize efficacy and minimize side effects
Pharmacogenomics study of how genetic variations influence drug response and toxicity
Cancer research understanding the genetic and epigenetic alterations that contribute to cancer development and progression
Oncogenes genes that, when mutated or overexpressed, can promote cancer growth (RAS, MYC)
Tumor suppressor genes genes that normally regulate cell growth and division, but when mutated or silenced, can lead to cancer (p53, RB)
Stem cell research study of cells that have the ability to self-renew and differentiate into specialized cell types
Embryonic stem cells pluripotent cells derived from early-stage embryos that can give rise to all cell types in the body
Induced pluripotent stem cells (iPSCs) adult cells reprogrammed to a pluripotent state by introducing specific transcription factors
Potential applications include regenerative medicine, disease modeling, and drug screening