Central Dogma
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Questions and Answers

Why is only one strand of the double-stranded DNA helix used as a template for replication?

Using only one strand ensures accurate replication by providing a direct template, preventing errors that could arise from combining information from both strands. Using both strands would cause conflicting information.

How does the absence of a nucleus in mature red blood cells relate to their primary function?

The absence of a nucleus allows more space for hemoglobin, maximizing oxygen transport capacity. Also, without a nucleus, the red blood cell cannot divide.

Explain why prokaryotes do not require intron removal like eukaryotes.

Prokaryotes lack introns in their genes, thus intron removal is unnecessary. Their genes are continuous coding sequences.

Describe the role PolyA tail length plays in mRNA stability and translation.

<p>A longer polyA tail increases mRNA stability and promotes translation by protecting the mRNA from degradation in the cytosol. A shorter tail leads to faster mRNA degradation and less protein synthesis.</p> Signup and view all the answers

Why is mRNA single-stranded while DNA is double-stranded?

<p>mRNA is single-stranded to allow it to exit the nucleus and to be easily accessed by ribosomes for translation. DNA is double-stranded for stability and accurate replication/storage of genetic information.</p> Signup and view all the answers

What is the purpose of adding a modified guanine nucleotide (capping) at the 5' end of mRNA during processing?

<p>The 5' cap protects the mRNA from degradation, enhances translation efficiency by aiding ribosome binding, and facilitates splicing of introns.</p> Signup and view all the answers

How can alternative splicing of a single gene lead to the production of different proteins?

<p>Alternative splicing involves selecting different combinations of exons, resulting in various mRNA transcripts that code for distinct proteins with potentially different functions.</p> Signup and view all the answers

Explain how mRNA degradation in the cytosol is related to the extent of protein synthesis.

<p>mRNA degradation limits the duration of protein synthesis. The more rapidly mRNA degrades, the shorter the period it is available for translation, thus limiting the amount of protein produced.</p> Signup and view all the answers

Why do proteins with a membrane destination go to the Rough Endoplasmic Reticulum (RER)?

<p>Proteins destined for membranes contain signal sequences that direct them to the RER for proper folding, modification, and insertion into the lipid bilayer.</p> Signup and view all the answers

If a mutation changed the start codon AUG to AUU in an mRNA, what would be the likely effect on translation?

<p>Translation would likely not occur or start at a different location in the mRNA as the start codon AUG, which codes for methionine, is essential for initiating protein synthesis.</p> Signup and view all the answers

Explain, generally, how a change in the amino acid sequence of a protein can alter its overall shape and function.

<p>The amino acid sequence determines the protein's folding and 3D structure. Different amino acids have different properties, so altering the sequence can disrupt these interactions, changing the resulting shape and function.</p> Signup and view all the answers

Describe the role of pyrophosphatase in the context of nucleotide addition during DNA or RNA synthesis.

<p>Pyrophosphatase hydrolyzes pyrophosphate (PPi), released during nucleotide addition, into two inorganic phosphate molecules (Pi). This exergonic reaction drives the polymerization process forward by making it irreversible.</p> Signup and view all the answers

During translation, what is the role of the small ribosomal subunit and the large ribosomal subunit?

<p>The small subunit binds to the mRNA and recruits the initiator tRNA, while the large subunit catalyzes peptide bond formation between amino acids. The mRNA binds on the small subunit, and the large subunit has binding sites for tRNA.</p> Signup and view all the answers

How can some antibiotics that target protein synthesis in prokaryotes be ineffective against eukaryotic cells?

<p>These antibiotics often target unique structural features of prokaryotic ribosomes (e.g. different rRNA sequences, unique proteins), which are distinct from eukaryotic ribosomes, therefore they do not affect eukaryotic protein synthesis.</p> Signup and view all the answers

Explain how a mutation in an enhancer region far from a gene can still impact protein synthesis.

<p>Enhancers regulate transcription by binding transcription factors that influence RNA polymerase activity at the promoter. A mutation can disrupt transcription factor binding, reducing or abolishing gene expression and protein synthesis.</p> Signup and view all the answers

Flashcards

Transcription

RNA synthesis using a DNA template to code for a single strand.

Nucleus

A cellular component containing the cell's genetic material.

Introns

Non-coding sections of pre-mRNA that are removed during RNA splicing.

Polyadenylation

The addition of multiple Adenine bases to the 3' end of an mRNA molecule, influences mRNA longevity.

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Promoter Region

Directs RNA polymerase where to begin transcription.

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5' Capping

A modified guanine nucleotide added to the 5' end of mRNA, important for processing.

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Cytosol

The location in the cell where protein synthesis takes place.

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Translation

The process of ribosomes using mRNA to synthesize proteins.

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Start Codon

The start codon AUG which codes for methionine and begins protein synthesis.

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Stop Codons

Specific sequences (UAA, UAG, UGA) that signal the end of translation.

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tRNA

Transfer RNA; carries amino acids to the ribosome during protein synthesis.

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Antibiotics and Protein Synthesis

Antibiotics can disrupt protein synthesis in prokaryotes.

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Termination Factors

Proteins that bind to ribosomes during translation termination.

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Ferritin

A protein that stores iron, preventing the buildup of toxic free radicals.

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Mutation

Changes or alterations that occur in the genetic sequence. These mutations can either impede or enhance protein synthesis.

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Study Notes

Central Dogma: DNA

  • Nucleic acids are the biomolecule basis, specifically deoxyribonucleic acid (DNA) and ribonucleic acid (RNA).
  • DNA forms the inherited genetic material inside cells, where segments known as genes code for protein synthesis and determine physical traits.
  • DNA doesn't directly control protein synthesis but uses RNA as an intermediate.

DNA Structure: Nucleotides

  • Nucleotides have three components.
  • Nitrogenous bases come in two types: Purines (double-ring) and Pyrimidines (single-ring).
  • DNA's 3D structure is a double helix.
    • The sugar-phosphate backbone forms a right-handed helix, maximizing base-pairing efficiency.
    • A complete turn occurs every 10 base pairs.
    • Two DNA strands are held together by hydrogen bonds between bases: Adenine (A) pairs with Thymine (T), and Guanine (G) pairs with Cytosine (C).
    • The number of purines must equal the number of pyrimidines to maintain the DNA double helix. - H bonds form between A and T, G and C.
  • Forces needed to stabilize the DNA double helix are hydrogen bonds, the sugar-phosphate backbone, and base stacking: - Bases stack parallel and expel water through hydrophobic effects.
  • Nucleotides are joined along the sugar phosphate backbone, this is known as phosphodiester bonds.
    • Positively charged magnesium ions help stabilize the negative charges found in the sugar phosphate backbone.

DNA Condensation

  • Nucleosomes, the structural unit for packaging DNA, consist of base pairs wrapped around a histone core known as protein octamer (H2A, H2B, H3, H4), and the H1 linker protein.
  • Chromatin, a complex of tightly bound protein and DNA, exists as densely packed heterochromatin or dispersed euchromatin:
    • Euchromatin being transcriptionally active.
  • DNA is packaged into chromosomes in condensed form. Human cells typically have 23 pairs of chromosomes (46 total), with one copy from each parent, called diploid (2n).
    • Maternal and paternal chromosome pairs are called homologous chromosomes.
  • Autosomal chromosomes, numbered 1-22, form homologous pairs.
  • Sex chromosomes determine biological sex:
    • Females have two X chromosomes, while males have one X and one Y chromosome.

Genes

  • Chromosomes carry genes that are the functional units of heredity.
  • A gene is a DNA segment containing instructions for making a particular protein.
  • An exon is a coding sequence of a gene.
  • An intron is a non-coding sequence of a gene.
    • Introns are removed via splicing after transcription.
  • 98.5% of the human genome is non-coding DNA, playing regulatory roles.
    • Promotor and enhancer regions bind transcription factors.
    • Binding sites organize chromatin structures.
    • Non-coding regulatory RNA includes microRNA.
    • Certain mobile genetic elements called transposons, are implicated in gene regulation and chromatin.

Central Dogma: RNA

  • RNA is a polymer of nucleotides linked by a phosphodiester bond, similar to DNA, but also different from DNA chemically in two ways.
    • There is ribose sugar instead of deoxyribose sugar.
    • Uracil (U) is used, rather than Thymine (T).
    • Adenine, guanine, and cytosine is still contained within the bonds

Structural Difference

  • Structurally, the molecules different.
  • DNA always occurs in a double-stranded helix
  • RNA is single-stranded
    • This allows it to fold up into various shapes

Functional Difference

  • mRNA is the template for protein translation.
    • This is called messenger RNA.
    • Initially called pre-mRNA.
    • Undergoes processing before maturing. .Some DNA sequences transcribed into RNA are not tranlated into proteins
    • This is called non-coding RNA.
    • Serves as regulatory, structural and enzymatic structural components.
  • snRNA, or small nuclear RNA is used in the spliceosome
    • Necessary to remove introns in the pre-mRNA, then splicing occurs.
    • Associates with protein subunits in order to form small nuclear ribonucleoproteins (snRNPs). This forms the core of the spliceosome.

Other forms of RNA

  • rRNA stands for Ribosomal RNA
    • Necessary for the basic structure of the ribosome
    • It has a large (60S) and small (40S) subunit
    • Involved in catalysis of the peptide bond between amino acids
  • tRNA transfer RNA
    • Needed in translation in order to carry the correct acid to the growing polypeptide change
    • The unique clover leaf shape has two key components
      • Anticodon, that pairs with the complementary code in it's mRNA
      • Amino acid binding site, a short single-stranded region at the 3' end that binds the corresponding anti-codon on the tRNA

###Wobble Theory

  • Theory: Despite there being 64 possible combinations of nucleotides in a 3 nucleotide codon ,there are only 20 amino acids
    • There is more than one possible tRNA for many of the amino acids.
    • This mean some molecules can pair with more than one codon
  • This causes the wobble theory, where two tRNA are built to only require accurate pair of only the first two positions in a codon.
    • These can tolerate mismatch and so many codons for an amino acid differ in their 3rd nucleotide.

###Non-coding other

  • miRNA or micro RNA is non-coding and helps regulate expression via post-transcriptional silencing
    • Prevents translation through promotion of degradation.
  • siRNA is small interering RNA which works to express gene expression
    • Through the direct degradation of mRNA.
  • IncRNA are long- non-coding RNA, which express gene expression
    • These help increase transcription
    • Involved in X-chromosome

Class

  • Chromosomes provide the functional unit of heredity.
  • 1st and 2nd steps of Eukaryotic transcription are defined as.
    • First the pre-mRNA will be transcribed.
    • Then 3 main ways of protein will occur through processing.

RNA

  • Transcription is a key process, using RNA made from a DNA molecules to help dictate of a protein is synthesized.
    • Takes place inside of the Nucleus of a cell.
  • Genes contains regulatory and Basal Promoter reasons, as well as transcription Start and EXONS
  • Prokaryates do not have Introns.
    • Coding reasons will transfer to RNA to help form transcription.
  • RNA Polymerase is very significant as an enzyne to start transcription.
    • It helps to unwind Double Helix to polymerization with a Phosphiester bond
    • RNA Polymerase Il helps to to take form MRA

Basic information.

  • Transcription has 3 basis step.
    • Gerenal Transcription
      • DNA to help startTranscription process.
      • Then area must help start signials. -Enlongation
      • RNS Polyremuse, catalzyes from addition to, prem RNA trancrpt
      • This occurs for MRMA is single stranded -Temination
      • pre—m RNA transfer and released from RNA polymease
      • Then is the final release to RNS and DNRA polymeasie

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Central Dogma Combined PDF

Description

Explore fundamental concepts in molecular biology. This includes DNA replication, mRNA processing, protein synthesis and the impact of genetic mutations. Learn about the central dogma and gene expression.

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