Ch 13.2, 13.3, 14.1, 14.2, 14.4 Genetics (DNA and RNA)

Learning Objectives Review: DNA, RNA, and Genetics

1. Role of DNA in Heredity (3 functions)

  • Storage of Genetic Information: DNA contains the instructions for building and maintaining an organism.

  • Replication: DNA can make exact copies of itself to pass genetic information to new cells.

  • Gene Expression: DNA sequences are used to make RNA and proteins, which determine traits.

2. Chemical Components of DNA

  • Nucleotides: Building blocks made of:

    • Sugar: Deoxyribose

    • Phosphate group

    • Nitrogenous bases: Adenine (A), Thymine (T), Guanine (G), Cytosine (C)

  • Bases pair specifically: A with T (2 hydrogen bonds), G with C (3 hydrogen bonds).

3. Role of DNA Polymerase in Copying DNA

  • Enzyme that adds complementary nucleotides to the original DNA strand during replication.

  • Proofreads and corrects errors to ensure accurate copying.

4. How DNA Differs from RNA

Feature

DNA

RNA

Sugar

Deoxyribose

Ribose

Bases

A, T, G, C

A, U (uracil), G, C

Strands

Double-stranded helix

Single-stranded

Function

Stores genetic info

Transfers info for protein synthesis

5. How the Cell Makes RNA (Transcription)

  • RNA polymerase binds to the promoter on DNA.

  • It unwinds DNA and assembles RNA nucleotides complementary to the DNA template.

  • RNA strand is processed (introns removed, exons spliced) before leaving the nucleus.

6. How the Genetic Code Works

  • Genetic code is read in codons (sets of 3 bases).

  • Each codon specifies an amino acid or a stop signal during protein synthesis.

  • Code is universal and redundant (multiple codons can code for the same amino acid).

7. Role of the Ribosome in Protein Assembly

  • Ribosomes read mRNA codons.

  • tRNA molecules bring specific amino acids matching the codon’s anticodon.

  • Ribosome links amino acids into a polypeptide chain (protein).

8. How Mutations Change Genetic Information

  • Mutations are changes in DNA sequence.

  • Types:

    • Point mutation: Change in a single base.

    • Frameshift mutation: Insertions or deletions that shift the reading frame.

  • Mutations can be caused by errors during replication or environmental factors (mutagens).

9. How Mutations Affect Genes

  • Can alter protein structure/function.

  • May have no effect (silent mutation), harmful effects, or occasionally beneficial traits.

  • Can lead to genetic diseases or increased variation in populations.

10. Cause and Effect: DNA, Chromosomes, and Traits

  • DNA is tightly packed into chromosomes.

  • Chromosomes carry genes, the instructions for traits.

  • Offspring inherit chromosomes from parents, passing traits via DNA sequences.

11. Cause and Effect: DNA, Proteins, and Traits

  • Genes (DNA) code for proteins.

  • Proteins perform functions or form structures that result in observable traits.

  • Changes in DNA affect proteins, which can alter traits.

12. Regulation of DNA Expression (Introns, Exons, etc.)

  • Genes contain exons (coding regions) and introns (non-coding).

  • Introns are removed in RNA processing.

  • Regulation of which exons are included affects which proteins are made (alternative splicing).

13. Genetic Variation from Meiosis Errors or Mutations

  • Meiosis errors: Nondisjunction can cause abnormal chromosome numbers (e.g., polyploidy).

  • Mutations from environmental mutagens can introduce new genetic variations.

  • These variations contribute to diversity and evolution.


Key Terms Summary

  • Base pairing: A-T (DNA), A-U (RNA), G-C

  • Complementary: Bases pair in a specific way

  • Nitrogenous bases: A, T, G, C, U (RNA)

  • Nucleic acid: DNA and RNA molecules

  • Nucleotide: Sugar + phosphate + base

  • Double helix: DNA structure of two strands twisted

  • Antiparallel strands: DNA strands run in opposite directions

  • Replication: DNA copying process

  • DNA polymerase: Enzyme for replication

  • Hydrogen bonds: Bonds between bases

  • Covalent bonds: Bonds in sugar-phosphate backbone

  • Sugar-phosphate backbone: Structural framework of DNA/RNA

  • Helicase: Enzyme that unwinds DNA

  • RNA: Ribonucleic acid, involved in protein synthesis

  • mRNA: Messenger RNA carrying code from DNA

  • rRNA: Ribosomal RNA, part of ribosome

  • tRNA: Transfer RNA, carries amino acids

  • Transcription: Making RNA from DNA

  • RNA polymerase: Enzyme that synthesizes RNA

  • Promoter: DNA region where RNA polymerase binds

  • Intron: Non-coding RNA section removed during processing

  • Exon: Coding RNA section kept in mature mRNA

  • Mutations: Changes in DNA sequence

  • Point mutation: Single base change

  • Frameshift mutation: Insertion/deletion changing reading frame

  • Mutagen: Agent causing mutations

  • Polyploidy: Having extra sets of chromosomes

  • Translation: Making protein from mRNA

  • Codon: Three-base sequence in mRNA coding for amino acid

  • Anticodon: tRNA sequence complementary to codon

  • Amino acid: Building block of proteins

  • Genes and proteins: Genes code for proteins

  • Polypeptide → protein: Chain of amino acids folds into functional protein

  • Central dogma of biology: DNA → RNA → Protein


Review Tip: Compare Replication, Transcription, and Translation

Process

Purpose

Location

Key Enzymes

Product

Replication

Copy DNA

Nucleus

DNA polymerase

DNA

Transcription

Make RNA from DNA

Nucleus

RNA polymerase

mRNA

Translation

Make protein from mRNA

Cytoplasm (ribosome)

Ribosome, tRNA

Polypeptide/protein