mRNA acts as a messenger that copies and transports genetic information from DNA to ribosomes for protein synthesis.
The process of using mRNA to synthesize proteins is known as translation.
DNA contains genes that code for proteins. Only relevant genes are transcribed into mRNA as needed by the cell.
RNA Polymerase is an enzyme that binds the DNA at the gene's start point to begin transcription.
mRNA is synthesized based on the template strand of DNA, which is complementary to the coding strand.
E.g., if the coding strand has the sequence ACGTA, the mRNA will have the complementary sequence UGCAU (with 'U' replacing 'T').
RNA Polymerase continues to add nucleotides to the growing mRNA strand until it reaches a terminator sequence on the DNA.
The terminator signals the end of transcription, and RNA Polymerase detaches from the DNA.
After synthesis, mRNA exits the DNA template. The DNA returns to its helical shape for further usage.
mRNA undergoes several modifications before it exits the nucleus:
Introns (non-coding sequences) are spliced out, and exons (coding sequences) are joined together.
A 5' cap and a poly-A tail are added to protect the mRNA from degradation during transportation to the ribosome.
The genetic code is universal across all organisms and consists of codons (triplet sequences of bases) which code for specific amino acids.
Out of approximately 64 codons, 20 correspond to amino acids with redundancy; some amino acids are specified by multiple codons.
AUG is the start codon, while UAA, UAG, and UGA are stop codons.
Transfer RNA (tRNA) carries amino acids to the ribosome where they match with the mRNA codons through complementary anticodons.
The interaction is crucial, as the tRNA must fit precisely to deliver the right amino acid.
In the ribosome, mRNA is read in sets of three codons, and tRNAs deliver corresponding amino acids, leading to the formation of a polypeptide chain through peptide bonds.
As each tRNA brings its amino acid, they are linked together by peptide bonds to form a growing protein chain.
This process continues until a stop codon is read, signaling the end of protein synthesis.
The newly synthesized polypeptide chain will fold into a specific three-dimensional structure critical for its function.
Mutations are changes in the DNA sequence that can occur during replication or as a result of external factors (e.g., radiation, chemicals).
Types of Mutations:
Silent Mutations: No change in the amino acid sequence; often occur due to redundancy in the genetic code.
Missense Mutations: Replace one amino acid in a polypeptide with another, potentially altering protein function.
Nonsense Mutations: Introduce a premature stop codon, resulting in truncated proteins, which usually lead to loss of function.
Frameshift Mutations: Caused by insertions or deletions of nucleotides; can drastically change the resulting protein sequence and function.
Composed of a phospholipid bilayer facilitating selective permeability.
Integral (transmembrane) proteins and peripheral proteins assist in transport and communication across the membrane.
Passive Transport: No energy required; substances move along a concentration gradient (high to low concentration).
Diffusion: Movement of molecules until equilibrium is reached. Factors influencing diffusion:
Distance (further distances slow down diffusion).
Molecule Size (smaller molecules diffuse faster).
Temperature (increased temperature speeds up diffusion).
Concentration Gradient (larger differences speed up diffusion).
Active Transport: Requires energy (usually ATP) to move substances against their concentration gradients (low to high concentration).
e.g., Sodium-Potassium pump, which actively transports sodium out and potassium into the cell.
Vesicular Transport (Active Transport): Includes endocytosis (bulk transport into the cell) and exocytosis (bulk transport out of the cell).
Phagocytosis: Cell 'eating', bringing in solid material.
Pinocytosis: Cell 'drinking', bringing in liquid.
Tonicity: Refers to the ability of a solution to cause a cell to gain or lose water.
Isotonic Solutions: Concentrations of solute equal inside and outside the cell; no net gain/loss of water.
Hypotonic Solutions: Lower solute concentration outside, leading to water influx and potential cell lysis (rupture).
Hypertonic Solutions: Higher solute concentration outside, causing water efflux and cell shrinkage (crenation).
The central dogma of molecular biology involves the flow of genetic information from DNA to RNA to protein.
Understanding the processes of transcription and translation, as well as mutation impact, is crucial for comprehension of genetic expression and cell function.