Genes, Genomes and Cell Structure
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Consider a mutation that disrupts the function of the spliceosome in a eukaryotic cell. What is the most likely direct consequence of this mutation on gene expression?

  • Increased rate of transcription initiation due to the accumulation of unprocessed mRNA.
  • Production of non-functional proteins due to the presence of introns in the mature mRNA. (correct)
  • Enhanced stability of mRNA molecules in the cytoplasm due to defective polyadenylation.
  • Premature termination of translation caused by the absence of the 5' cap structure.

In a hypothetical scenario, a novel prokaryotic organism is discovered whose transcriptional machinery utilizes a sigma factor with altered specificity. This altered sigma factor preferentially binds to promoter regions with a modified consensus sequence. How would this impact the organism's gene expression profile under varying environmental conditions?

  • Random and unpredictable gene expression patterns, leading to cellular dysfunction and eventual cell death.
  • Global up-regulation of all genes, as the altered sigma factor enhances transcription initiation indiscriminately.
  • Complete cessation of transcription due to incompatibility of the altered sigma factor with the core RNA polymerase enzyme.
  • Selective expression of a distinct set of genes regulated by the modified promoter sequence, allowing for adaptation to specific environmental niches. (correct)

A researcher is investigating a novel regulatory mechanism in eukaryotic transcription. They discover a noncoding RNA (ncRNA) molecule that binds directly to an enhancer sequence, preventing the binding of transcription factors. How would this ncRNA likely influence the expression of the target gene?

  • Repress gene expression by blocking the binding of transcription factors to the enhancer, thereby reducing transcription initiation. (correct)
  • Induce epigenetic modifications, leading to long-term activation of the target gene regardless of environmental signals.
  • Have no effect on gene expression, as enhancers function independently of transcription factors and ncRNA molecules.
  • Enhance gene expression by promoting chromatin remodeling and increasing accessibility of the enhancer sequence.

A scientist is studying a gene in yeast and discovers that a specific mutation leads to the production of a primary transcript that is significantly longer than the wild-type transcript. Further analysis reveals that the polyadenylation signal sequence is mutated. What is the most likely consequence of this mutation?

<p>Failure to properly cleave and polyadenylate the 3' end of the transcript, leading to an extended and potentially unstable mRNA. (C)</p> Signup and view all the answers

Imagine a scenario where a cell is exposed to a chemical that inhibits the function of aminoacyl-tRNA synthetases. How would this chemical most directly affect protein synthesis?

<p>It would prevent the charging of tRNA molecules with their corresponding amino acids. (A)</p> Signup and view all the answers

A researcher is investigating a novel antibiotic that specifically targets bacterial translation. They discover that the antibiotic binds to the 23S rRNA within the large ribosomal subunit. What is the most likely mechanism of action of this antibiotic?

<p>Prevention of peptidyl transferase activity, blocking peptide bond formation. (D)</p> Signup and view all the answers

In a cell undergoing active translation, what would be the immediate consequence of depleting the available pool of GTP (guanosine triphosphate)?

<p>Arrest of ribosome translocation along the mRNA, preventing further codon reading. (C)</p> Signup and view all the answers

In the context of DNA replication, which of the following scenarios would MOST critically impede the progression of the lagging strand synthesis, assuming all other enzymatic functions remain unimpaired?

<p>A deficiency in RNA primase activity, resulting in a 75% reduction in primer synthesis. (B)</p> Signup and view all the answers

Consider a newly discovered genetic element within the 3' untranslated region (UTR) of a specific mRNA molecule that recruits a protein complex capable of degrading the mRNA. How would the presence of this element most likely affect gene expression?

<p>Reduced protein synthesis due to decreased mRNA half-life and accelerated degradation. (C)</p> Signup and view all the answers

A researcher is investigating a novel mutation in a cell line that disrupts the normal progression of DNA replication. Upon closer inspection, they observe that while the leading strand synthesis proceeds relatively unimpeded, the lagging strand exhibits a significantly reduced rate of Okazaki fragment maturation. Which of the following mutations would be MOST likely to cause this specific phenotype?

<p>A mutation in the gene encoding DNA ligase that reduces its affinity for ATP. (A)</p> Signup and view all the answers

Consider a scenario where a nascent mRNA transcript is undergoing processing in the nucleus of a eukaryotic cell. A specific point mutation occurs within the promoter region of the corresponding gene, subtly altering the binding affinity of RNA polymerase. Which of the following outcomes would be the MOST probable consequence of this mutation?

<p>An altered rate of transcription initiation, potentially leading to either increased or decreased mRNA transcript abundance. (D)</p> Signup and view all the answers

In a hypothetical scenario, a novel chemical compound selectively inhibits the activity of DNA helicase in eukaryotic cells. Assuming that all other DNA replication enzymes function optimally, what would be the MOST immediate and direct consequence of applying this compound to actively dividing cells?

<p>Inhibition of DNA replication initiation and progression, resulting in cell cycle arrest. (A)</p> Signup and view all the answers

Scientists are analyzing a newly discovered viral genome. They observe that the viral genome consists of RNA, but lacks a gene encoding RNA primase. Which of the following mechanisms would the virus MOST likely employ to initiate replication of its genome within a host cell?

<p>The virus utilizes the host cell's RNA primase to synthesize primers on the viral RNA template sequence. (B)</p> Signup and view all the answers

Consider a eukaryotic cell undergoing DNA replication. A researcher introduces a modified nucleotide analog that is readily incorporated into newly synthesized DNA but lacks a 3'-OH group. What would be the MOST immediate consequence of incorporating this analog during DNA replication?

<p>Elongation of the DNA strand would be prematurely terminated upon incorporation of the analog. (A)</p> Signup and view all the answers

Imagine a scenario where a mutation occurs in the promoter region of a gene, specifically disrupting the consensus sequence recognized by a key transcription factor. Which of the following outcomes would be the MOST likely consequence of this mutation on gene expression?

<p>A change in the rate of transcription initiation, potentially leading to either up- or down-regulation of gene expression. (E)</p> Signup and view all the answers

A researcher is studying a novel DNA polymerase isolated from an archaeal species. Through in vitro assays, they determine that this polymerase lacks 5' to 3' exonuclease activity. How would the absence of this activity MOST directly affect Okazaki fragment processing during DNA replication in this archaeon?

<p>The RNA primers at the 5' ends of Okazaki fragments would not be efficiently removed. (C)</p> Signup and view all the answers

Considering the nuanced differences in transcriptional regulation between prokaryotes and eukaryotes, which statement MOST accurately reflects the functional divergence of transcription factors in these two domains of life?

<p>Prokaryotic transcription factors primarily modulate gene expression by directly interacting with RNA polymerase to initiate or repress transcription, while eukaryotic transcription factors often act indirectly via chromatin modification and enhancer-mediated interactions. (A)</p> Signup and view all the answers

In a hypothetical scenario, a novel lncRNA is discovered and found to interact with a specific mRNA transcript, leading to a significant decrease in protein production. Based on current understanding, which mechanism MOST likely explains the action of this lncRNA?

<p>The lncRNA facilitates the degradation of the mRNA transcript by recruiting ribonucleases to the site of interaction, leading to its rapid turnover. (C)</p> Signup and view all the answers

Assume a bacterial cell experiences a mutation that disrupts the operator region of a repressible operon. Which consequence is MOST likely to occur?

<p>The structural genes within the operon will be transcribed constitutively, irrespective of the presence or absence of the corepressor (D)</p> Signup and view all the answers

Within the context of eukaryotic gene regulation, enhancers play a pivotal role. Which mechanism BEST describes the interaction between enhancers and promoters?

<p>Enhancers, often located distal to the gene they regulate, interact with the promoter via DNA looping, facilitated by mediator complexes and transcription factors, to modulate gene expression. (B)</p> Signup and view all the answers

In the realm of RNA interference (RNAi), both siRNAs and miRNAs play crucial roles in gene silencing. What is the key distinction in their biogenesis and target specificity?

<p>siRNAs are processed from long double-stranded RNA precursors and typically exhibit perfect complementarity to a single mRNA target, leading to mRNA degradation, whereas miRNAs are transcribed from specific gene loci and possess imperfect complementarity to multiple mRNA targets, resulting in translational repression or mRNA destabilization. (C)</p> Signup and view all the answers

Consider a synthetic biology experiment where an artificial operon is constructed in E. coli. This operon contains a novel regulatory sequence that binds a synthetic repressor protein with exceptionally high affinity, even in the presence of a typical inducer molecule. What outcome is MOST probable?

<p>The operon will remain constitutively repressed, as the high-affinity repressor effectively overrides the inducer's effect. (C)</p> Signup and view all the answers

Investigating the effects of a novel epigenetic drug on gene expression, it is observed that the drug selectively demethylates cytosine residues within the promoter regions of tumor suppressor genes. Predict the MOST likely downstream consequence of this drug's action.

<p>Activation of tumor suppressor gene expression, potentially leading to cell cycle arrest, apoptosis, or reduced tumor growth. (A)</p> Signup and view all the answers

In a study examining translational regulation, a researcher discovers a novel RNA-binding protein (RBP) that binds to the 5' untranslated region (UTR) of a specific mRNA transcript. This binding event is found to be highly sensitive to intracellular iron concentrations. Under conditions of low intracellular iron, what is the MOST plausible outcome of RBP binding?

<p>Inhibition of ribosome scanning and translation initiation, resulting in reduced protein synthesis. (A)</p> Signup and view all the answers

Consider a bacterial cell undergoing rapid growth in an environment with plentiful lactose. A mutation arises that completely disables the lacA gene. Which of the following scenarios is the MOST likely immediate consequence within this cell?

<p>The cell will accumulate toxic metabolic byproducts due to impaired processing of thiogalactosides, inhibiting growth. (B)</p> Signup and view all the answers

A researcher is studying a novel bacterial species and identifies a gene with significant homology to the lacI gene of E. coli. However, unlike E. coli, the expression of this operon is constitutive, irrespective of the presence or absence of lactose. Which of the following mutations in the lacI homolog is MOST likely to explain this observation?

<p>A missense mutation in the DNA-binding domain of the <em>lacI</em> homolog prevents it from binding to the operator sequence. (A)</p> Signup and view all the answers

In a population of bacteria, a subset exhibits increased resistance to a novel antibiotic. Whole-genome sequencing reveals that these resistant bacteria share a previously unknown mutation in a gene encoding a ribosomal protein. Further analysis reveals that this mutation does not alter the amino acid sequence of the protein. Which of the following mechanisms BEST explains how this silent mutation confers antibiotic resistance?

<p>The mutation alters the codon bias, leading to a conformational change in the ribosome that reduces the antibiotic's affinity. (B)</p> Signup and view all the answers

A geneticist is studying a human disease caused by a frameshift mutation in a critical metabolic enzyme. They identify two patients: one with a deletion of a single nucleotide early in the coding sequence and another with an insertion of two nucleotides near the end of the coding sequence. Which patient is MORE likely to exhibit a milder phenotype, assuming no compensatory mechanisms are in play?

<p>The patient with the insertion near the end of the coding sequence, as the majority of the protein's functional domains will be correctly translated. (A)</p> Signup and view all the answers

A researcher discovers a novel chemical mutagen that induces primarily transition mutations (purine to purine or pyrimidine to pyrimidine). If this mutagen is applied to a population of bacteria, which of the following genes is MOST likely to accumulate loss-of-function mutations at the HIGHEST rate?

<p>A gene where a single base change can easily generate a stop codon. (A)</p> Signup and view all the answers

A researcher is studying a newly discovered epigenetic mark and observes that it consistently correlates with transcriptional repression. Which of the following experimental approaches would provide the MOST direct evidence that this epigenetic mark is causally involved in gene silencing, rather than merely correlated with it?

<p>Developing a method to specifically remove the epigenetic mark from a target gene and observing a corresponding increase in transcription. (D)</p> Signup and view all the answers

In a clinical trial for a novel gene therapy targeting a specific inherited metabolic disorder, some patients exhibit a therapeutic response while others do not. Subsequent analysis reveals that the non-responsive patients have a particular SNP within an intron of the targeted gene, distant from any known splice sites. What is the MOST plausible explanation for why this intronic SNP is affecting the outcome of gene therapy?

<p>The SNP affects the binding affinity of RNA-binding proteins involved in mRNA stability or export, leading to reduced levels of the therapeutic transcript. (D)</p> Signup and view all the answers

You are investigating a eukaryotic gene that is transcribed at high levels in liver cells but is silent in brain cells. You identify a DNA region 20kb upstream of the transcription start site that is heavily methylated in brain cells but unmethylated in liver cells. Furthermore, this region contains binding motifs for several known transcription factors. Which of the following is the MOST likely mechanism by which methylation of this region silences the gene in brain cells?

<p>Methylation recruits histone deacetylases (HDACs) and other chromatin remodeling factors, leading to chromatin condensation and reduced accessibility of the DNA to transcription factors. (B)</p> Signup and view all the answers

Consider a bacterial species exhibiting atypical cell wall characteristics, rendering it uniquely susceptible to lysis in hypotonic solutions despite possessing an intact plasma membrane. Which factor would MOST critically influence its survival in such conditions?

<p>The efficiency of efflux pumps in regulating intracellular ion concentrations against an osmotic gradient. (A)</p> Signup and view all the answers

In a hypothetical scenario where DNA polymerase exhibits a significantly reduced affinity for nucleotide triphosphates (NTPs), yet maintains robust proofreading capabilities, what would be the MOST immediate and observable consequence on cellular function?

<p>A substantial decrease in the overall rate of DNA replication, impacting cell division. (D)</p> Signup and view all the answers

Imagine a newly discovered prokaryotic organism thriving in extreme alkaline environments. Its DNA exhibits a novel modification wherein a subset of adenine bases are covalently modified with a bulky hydrophobic group. How might this modification MOST directly contribute to its survival?

<p>By shielding the phosphodiester backbone from hydroxyl ion attack, stabilizing DNA integrity in alkaline conditions. (A)</p> Signup and view all the answers

Consider a hypothetical situation where eukaryotic cells are engineered to lack the nuclear envelope. What compensatory mechanism, if any, would be MOST critical for the survival of these modified cells, assuming all other cellular functions remain intact?

<p>Spatial segregation of transcription and translation machineries within the cytoplasm, utilizing RNA granules. (D)</p> Signup and view all the answers

Suppose a researcher discovers a novel enzyme in eukaryotic cells that catalyzes the formation of an unusual phosphodiester bond between the 2' hydroxyl group of one nucleotide and the 5' phosphate group of the next. What would be the MOST immediate and significant consequence of incorporating this enzyme into DNA replication?

<p>Disruption of DNA replication fork progression, leading to stalled replication and genomic instability. (A)</p> Signup and view all the answers

Imagine a scenario in which a mutation occurs in a bacterial species, causing its ribosomes to lose the ability to discriminate between initiator and elongator tRNAs. What would MOST likely be the immediate consequence of this mutation on protein synthesis?

<p>Aberrant initiation of translation at internal AUG codons, leading to synthesis of non-functional or toxic proteins. (C)</p> Signup and view all the answers

Consider a hypothetical scenario where DNA ligase activity is completely abolished in a eukaryotic cell line. What would be the MOST direct and immediate consequence on DNA replication and genome integrity?

<p>Accumulation of single-stranded DNA breaks and stalled replication forks, leading to genomic instability. (B)</p> Signup and view all the answers

In a fictional scenario, scientists engineer a synthetic nucleotide containing a modified pentose sugar that lacks the 2' hydroxyl group, rendering it resistant to enzymatic degradation. If this nucleotide were incorporated into a replicating strand of DNA, what would be the MOST likely consequence?

<p>Prevention of further chain elongation due to the absence of a required substrate for phosphodiester bond formation. (C)</p> Signup and view all the answers

Consider a novel synthetic biology experiment where artificial nucleobases are incorporated into a DNA analogue. If this analogue follows a modified 'Chargaff's rule' where a novel base 'X' pairs with 'Y' and 'G' still pairs with 'C', but the ratio of (X+G)/(Y+C) is consistently 1.5 in all synthesized strands, what implications would this altered ratio have on the structural and replicative properties of the DNA analogue?

<p>The DNA analogue would exhibit impaired replication fidelity due to the disruption of consistent hydrogen bonding patterns, leading to increased mutation rates. (B)</p> Signup and view all the answers

In a hypothetical scenario, a eukaryotic cell undergoes mitosis but fails to properly segregate sister chromatids during anaphase. Instead, all sister chromatids migrate to one daughter cell, while the other daughter cell receives no chromosomes. Assuming this aberrant cell division occurs in a somatic cell, what is the most likely outcome for the resulting daughter cells?

<p>The daughter cell with the duplicated chromosome set will likely become polyploid and potentially undergo oncogenic transformation if cell cycle checkpoints are bypassed. (A)</p> Signup and view all the answers

Imagine a research team discovers a novel protein that specifically binds to telomeres in human cells, enhancing their stability and preventing telomere shortening during DNA replication. If this protein is overexpressed in somatic cells, what is the most likely long-term consequence?

<p>Uncontrolled cell proliferation and potential tumorigenesis due to the circumvention of replicative senescence. (A)</p> Signup and view all the answers

Consider a scenario where a novel mutagen causes random, but consistent, translocations between non-homologous chromosomes in a population of somatic cells. If these translocations do not directly disrupt essential genes, what is the most likely long-term consequence for the affected organism?

<p>A higher risk of developing various cancers due to the potential disruption of gene regulation and cell cycle control. (C)</p> Signup and view all the answers

Suppose a newly discovered enzyme selectively degrades the histone protein H1 in eukaryotic cells. What immediate effect would this enzyme likely have on chromosome structure and gene expression?

<p>Reduced chromatin compaction and increased accessibility of DNA to transcription factors, potentially leading to altered gene expression patterns. (B)</p> Signup and view all the answers

In a population of cancer cells, researchers identify a mutation that prevents the formation of the cohesin complex. What impact would this mutation likely have on cell division and genomic stability?

<p>Aberrant chromosome segregation during mitosis, leading to aneuploidy and increased genomic instability. (C)</p> Signup and view all the answers

Consider a scenario where a mutation in a gene encoding a key microtubule-associated protein (MAP) disrupts the proper formation of the mitotic spindle during cell division. What is the most likely consequence of this mutation on chromosome segregation and cell viability?

<p>Random chromosome segregation, aneuploidy, and potential cell death due to failure of the spindle assembly checkpoint. (A)</p> Signup and view all the answers

Imagine a novel form of karyotype analysis that uses fluorescent probes to simultaneously detect the presence and methylation status of specific DNA sequences on chromosomes. If this analysis reveals a consistent pattern of hypermethylation at pericentromeric regions on multiple chromosomes in a sample of tumor cells, what might this suggest about the cells' genomic stability and gene expression?

<p>Compromised centromere function, potentially leading to chromosomal instability and aneuploidy. (A)</p> Signup and view all the answers

Flashcards

DNA

Deoxyribonucleic acid, the genetic material in cells.

Genes

Segments of DNA that control cell activities and traits.

Prokaryotic Cells

Cells without a nucleus, such as bacteria.

Eukaryotic Cells

Cells with a true nucleus, including plant and animal cells.

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ATP

Adenosine triphosphate, the energy currency of the cell.

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Nucleotides

Building blocks of DNA, consisting of a sugar, phosphate, and base.

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Nitrogenous Bases

The four bases in DNA: adenine, thymine, guanine, and cytosine.

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Double Helix

The structure of DNA, forming a twisted ladder shape.

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Complementary base pairs

Pairs of nitrogenous bases in DNA: A/T and G/C.

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Chromosome

An organized structure of DNA and proteins, containing genes.

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Autosomes

Chromosomes that are not sex chromosomes; humans have 22 pairs.

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Haploid

The number of chromosomes in gametes, which is half of somatic cells.

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Diploid

The total number of chromosomes in somatic cells, usually 46 in humans.

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Sister chromatids

Identical copies of a chromosome, joined at the centromere.

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Telomere

The protective end of a linear chromosome, involved in aging.

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Spectral Karyotype

A method for detailed chromosome analysis using color probes.

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FISH

A technique to analyze chromosomes for structural changes.

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Mitosis

The process by which somatic cells divide to create two identical cells.

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Meiosis

The cell division process that produces gametes (sperm and egg cells).

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Zygote

The fertilized egg formed by the union of sperm and egg cells.

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Semiconservative Replication

DNA replication where each new DNA has one parental and one new strand.

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Genome

All of the DNA contained within a cell.

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Transcription

The process of making messenger RNA (mRNA) from DNA.

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Transcription Factors

Proteins that direct RNA polymerase binding on DNA.

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Enhancers

DNA sequences that help transcription factors direct RNA polymerase.

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Template Strand

The DNA strand used to create mRNA during transcription.

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Coding Strand

The opposite DNA strand to the template, similar to mRNA.

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RNA Splicing

Process of removing introns and linking exons in pre-mRNA.

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Alternative Splicing

Different exons of the same gene are combined to produce multiple proteins.

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5' Cap

A modified guanine added to the 5' end of mRNA during processing.

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Polyadenylation

The addition of a series of adenine nucleotides at the 3' end of mRNA.

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Gene Expression

The process by which a cell produces mRNA from a gene.

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Gene Regulation

The mechanisms that control when and how genes are expressed.

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Transcriptional Regulation

Control of gene expression at the transcription stage.

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Promoter

A DNA sequence where RNA polymerase binds to initiate transcription.

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TATA Box

A common promoter sequence found in eukaryotes crucial for transcription initiation.

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Noncoding RNAs

RNA molecules that do not code for proteins but play roles in gene regulation.

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Operon

A cluster of genes in bacteria that are regulated together as a unit.

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lac operon

A set of genes involved in lactose degradation, controlled by a repressor.

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lac repressor

A protein that binds to the operator and prevents transcription of the lac operon.

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mutation

A change in the nucleotide sequence of DNA.

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mutagen

An environmental factor that causes mutations, can be physical or chemical.

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point mutation

A common type of mutation affecting a single nucleotide, can be SNP.

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missense mutation

A mutation that changes one amino acid in a protein.

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nonsense mutation

A mutation that creates a stop codon, terminating protein synthesis prematurely.

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frameshift mutation

A mutation caused by insertions or deletions that alters the reading frame of a gene.

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Study Notes

Chapter 2: Introduction to Genes and Genomes

  • DNA is the foundation of biotechnology, it's replicated, and the processes of transcription and translation produce proteins.
  • Cells are the basic unit of life, varying in shape, size, and function. The genetic information in all cells is DNA. Genes control cellular activities and determine organismal traits.

2.1 A Review of Cell Structure

  • Prokaryotic Cells:

    • Lack a nucleus (Table 2.1)
    • Simple cell structure compared to eukaryotes (Fig. 2.1)
    • Have a plasma membrane and cytoplasm. Some have organelles.
    • Bacteria are prokaryotic.
  • Eukaryotic Cells:

    • Have a true nucleus (Fig. 2.2)
    • Include fungi, protists, plants, and animals (Fig 2.2).
    • Possess organelles like mitochondria (responsible for ATP production) and a nucleus (containing most DNA), surrounded by a nuclear envelope.
  • Cytoplasm consists of cytosol and organelles, with each organelle carrying out specific functions. (Table 2.2)

2.2 The Molecule of Life

  • DNA and RNA are the two major nucleic acids in cells.
  • DNA is the genetic material in cells, and its building blocks are nucleotides.
  • Nucleotides consist of a pentose sugar (deoxyribose), a phosphate group, and a nitrogenous base (adenine, thymine, guanine, cytosine) (Fig 2.3).
  • Watson and Crick determined the double helix structure of DNA (Fig 2.4) - strands are antiparallel and connected via phosphodiester bonds.
  • DNA is organized into chromosomes.

2.3 Chromosome Structure, DNA Replication, and Genomes

  • DNA is packaged into chromosomes.
  • In non-dividing cells, DNA is in a less compact chromatin state, while it condenses into chromosomes when the cell is ready to divide (Fig. 2.5).
  • Bacteria have a single circular chromosome. Eukaryotes have multiple linear chromosomes (23 pairs in humans, 1-22 being autosomes and 23rd being sex chromosomes X,Y (Fig 2.6)).
  • Somatic cells have a diploid (2n) number of chromosomes (46 in humans). Gametes (sperm and egg cells) have a haploid (n) number.
  • Chromosomes are copied (replicated) and produce sister chromatids attached at the centromere.
  • The centromere divides the chromosome into two arms (p and q).
  • The ends of the linear chromosome are telomeres.
  • Karyotyping is a method for analyzing chromosomes (Fig. 2.6).

2.4 RNA and Protein Synthesis

  • Genes direct the synthesis of proteins, which have various cellular functions.
  • Genes are transcribed into messenger RNA (mRNA).
  • mRNA is translated into proteins.
  • Ribosomes read mRNA codons to produce proteins.
  • RNA polymerase carries out transcription (Fig. 2.10)
  • mRNA processing occurs in eukaryotic cells where introns are removed and exons are joined together (Fig. 2.11).

2.5 Regulation of Gene Expression

  • Gene expression refers to the production of mRNA from DNA.
  • Cells regulate when a gene product is made.
  • Gene expression is controlled by several mechanisms including transcriptional, post-transcriptional, translational, and post-translational regulation.
  • Transcriptional regulation is about controlling transcription at the promoter sequence, which differ between prokaryotes and eukaryotes (prokaryotes have operons ; eukaryotes have TATA and CAT boxes Fig 2.14).
  • Transcription factors are important in eukaryotes that allow RNA polymerase to bind to the promoter, and enhancers help to regulate gene expression tightly.
  • Non-coding RNAs can also regulate gene expression (Table 2.4).

2.6 Mutations: Causes and Consequences

  • A mutation is a change in the DNA nucleotide sequence.
  • Mutations can be spontaneous or caused by mutagens including UV light (physical) and chemicals
  • Mutations can be silent (no change in amino acid), missense (change in an amino acid), nonsense (changes to a stop codon) or frameshift (caused by insertions or deletions).
  • Mutations can be inherited or acquired (acquired happen in somatic cells).
  • Mutations can lead to genetic variation and diseases like sickle cell anemia.

2.7 Revealing the Epigenome

  • The epigenome is the modification of chromosome structure without changing the DNA sequence (e.g., methylation of DNA).
  • Environmental factors and diet can influence the epigenome.

2.8 Immune Response Mechanism in Prokaryotes

  • CRISPR-Cas system in prokaryotes is used as an adaptive immune responses (Fig 2.21), used for gene editing.

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Explore the basics of genes, genomes, and cell structure. Learn about DNA replication, transcription, and translation in protein production. Compare prokaryotic and eukaryotic cells, focusing on their structures and functions.

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