Exam 3 Review
Exam 3 Review: Key Biological Concepts
Chromatin Structure
Euchromatin:
- Definition: Loose form of chromatin.
- Implication: Associated with ACTIVE genes.Heterochromatin:
- Definition: Tight form of chromatin.
- Implication: Associated with INACTIVE genes.
Chromosome Basics
Sister Chromatids:
- Definition: Identical copies of a chromosome.Centromere:
- Function: Holds sister chromatids together.Kinetochore:
- Function: Point where spindle fibers attach during cell division.Telomeres:
- Function: Protect the ends of DNA from degradation.
Gene Structure
Promoter:
- Definition: Region where transcription of a gene begins.Coding Region:
- Definition: Part of the gene that is transcribed into RNA and ultimately translated into protein.RNA Processing:
- Description: RNA is transformed from its initial transcribed form into a mature messenger RNA (mRNA) through several steps, such as capping, polyadenylation, and splicing.
Prokaryotic Genes
Monocistronic:
- Definition: Refers to mRNA that codes for a single protein (1 gene -> 1 protein).Polycistronic:
- Definition: Refers to mRNA that codes for multiple proteins (1 RNA -> Multiple proteins).Operons:
- Description: A cluster of genes transcribed together under the control of a single promoter. They often are involved in the same metabolic pathway or function.
DNA Methods
PCR (Polymerase Chain Reaction):
- Purpose: To amplify a specific DNA segment.
- Steps:
1. Denature: Separate the DNA strands by heating.
2. Primer Binding: Short DNA primers bind to their complementary sequences on the single-stranded DNA.
3. Extension: DNA polymerase synthesizes new DNA strands.
4. Result: Exponential growth of the target DNA region.Sanger Sequencing:
- Purpose: To determine the nucleotide sequence of DNA.
- Description: Utilizes dideoxynucleotides (ddNTPs) to terminate DNA chain elongation; results in fragments of different lengths that are then read to derive the sequence.Crispr:
- Purpose: To edit DNA within genomes.
- Mechanism: Guide RNA directs the Cas9 enzyme to the target DNA sequence where it creates a double-strand break, facilitating either the knockout of a gene or the insertion of new genetic material.Gel Electrophoresis:
- Description: A method used for separating DNA fragments based on their size.
- Principle: DNA moves toward the positive charge (+) in the gel; smaller fragments migrate faster than larger ones.Plasmids:
- Definition: Circular DNA molecules distinct from chromosomal DNA.
- Use: Commonly used in genetic engineering to insert foreign genes.
- Features: Contain an origin of replication and often carry genes for antibiotic resistance.
Carbohydrates
General Formula:
- CnH2nOn: Represents the chemical structure of carbohydrates.Primary Functions:
- Energy Storage: Provides fuel for cellular processes.
- Structural Components: Contributes to cellular structure (e.g., in plant cell walls).
- Cell Signaling: Plays a role in cell communication and recognition.
Types of Sugars
Aldose:
- Definition: A sugar with an aldehyde group in its structure (e.g., glucose).Ketose:
- Definition: A sugar containing a ketone group (e.g., fructose).
Identification of Sugars
D vs. L Configuration:
- Determination: Based on the orientation of the hydroxyl group (-OH) on the second to last carbon in the sugar molecule:
- D: OH group on the right.
- L: OH group on the left.
- Notably, most biological sugars are in the D configuration.Enantiomers:
- Definition: Mirror images of each other.Diastereomers:
- Definition: Stereoisomers that are not mirror images; differ at one or more carbon.Epimers:
- Definition: Stereoisomers that differ at exactly ONE carbon atom.
- Note: All epimers are diastereomers.
Chemistry of Sugars
Aldose:
- Forms hemiacetal upon cyclization.Ketose:
- Forms hemiketal upon cyclization.Anomeric Carbon:
- Definition: The carbon atom in a sugar that becomes a new stereocenter upon cyclization.
- Can represent α and β anomers depending on the orientation of the hydroxyl group.
Enzymes
Definition: Catalysts that speed up chemical reactions.
Function:
- Lower the activation energy (E_a) needed for reactions to occur.
- Enzymes do NOT change the overall energy of the reaction.
- Mechanism: Stabilize the transition state to make the reaction more favorable.