Heredity and Genetics Lesson: Mendel, Traits, and More

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Lesson Overview

Heredity is the process by which traits are passed from parents to offspring. Genetics is the scientific study of heredity and variation in living organisms. This field helps explain how characteristics such as eye color, height, or inherited disorders are transmitted through generations via genes.

Fundamental Genetic Vocabulary

A solid understanding of genetic terminology is necessary to interpret how traits are inherited.

  • Gene: A segment of DNA that carries instructions for the synthesis of proteins or the control of traits.
  • Allele: Different versions of a gene, located at the same locus on homologous chromosomes.
  • Genotype: The genetic composition of an organism for a specific trait, represented by allele combinations (e.g., TT, Tt, tt).
  • Phenotype: The physical expression or visible trait resulting from a genotype (e.g., tall or short).
  • Homozygous: Two identical alleles for a trait (TT or tt).
  • Heterozygous: Two different alleles for a trait (Tt).
  • Dominant Allele: An allele that expresses its effect even if only one copy is present.
  • Recessive Allele: An allele that is masked by the presence of a dominant allele and only expresses when two copies are present.

Mendel's Laws of Inheritance

Gregor Mendel discovered basic inheritance rules through pea plant experiments.

Law of Segregation

  • Each organism has two alleles for a trait.
  • These alleles segregate during gamete formation.
  • Each gamete receives only one allele.
  • Fertilization restores the pair in offspring.

Law of Independent Assortment

  • Alleles for different traits assort independently.
  • Inheritance of one trait does not affect the inheritance of another.

Dominant vs. Recessive Traits

Dominant and recessive interactions determine which traits are visible.

GenotypePhenotype (if T = tall, t = short)
TTTall
TtTall
ttShort
  • Dominant traits mask the effect of recessive traits.
  • Recessive traits appear only if both alleles are recessive.

Punnett Square Method

Punnett squares are used to predict possible offspring genotypes and phenotypes.

Example: Monohybrid Cross

Cross between Tt × Tt (Tall is dominant)

Tt
TTTTt
tTttt
  • Genotype ratio: 1 TT : 2 Tt : 1 tt
  • Phenotype ratio: 3 Tall : 1 Short

Interpretation

  • 75% of the offspring are tall.
  • 25% are short due to the homozygous recessive (tt) genotype.

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Dihybrid Crosses and Independent Assortment

Dihybrid crosses involve two traits and illustrate independent assortment.

Example: RrYy × RrYy

Where R = round, r = wrinkled; Y = yellow, y = green

RYRyrYry
RYRRYYRRYyRrYYRrYy
RyRRYyRRyyRrYyRryy
rYRrYYRrYyrrYYrrYy
ryRrYyRryyrrYyRryy
  • Phenotypic ratio: 9 round yellow : 3 round green : 3 wrinkled yellow : 1 wrinkled green

Sex-Linked Traits and X-Linked Inheritance

Some traits are located on sex chromosomes, especially the X chromosome.

X-Linked Recessive Inheritance

  • Males (XY) have only one X chromosome.
  • A single recessive allele on the X leads to the condition in males.
  • Females (XX) must inherit two copies to express the trait.

Example: Colorblindness

Parent GenotypesPossible Offspring
XcX × XY50% carrier daughters, 50% colorblind sons
XcX × XcY50% colorblind sons, 50% colorblind daughters
  • Xc = X chromosome with recessive allele for colorblindness.

Autosomes vs. Sex Chromosomes

Human chromosomes are divided into autosomes and sex chromosomes.

Chromosome TypeNumber in HumansFunction
Autosomes22 pairsCarry most genetic information
Sex Chromosomes1 pair (XX or XY)Determine biological sex
  • Genes located on autosomes affect both sexes equally.
  • Sex-linked traits are influenced by the specific X or Y chromosomes.

Phenotype vs. Genotype Analysis

Understanding the relationship between phenotype and genotype is essential.

GenotypePhenotypeType
TTTallHomozygous Dominant
TtTallHeterozygous
ttShortHomozygous Recessive
  • Genotype determines phenotype.
  • Environment can also influence phenotype expression.

Genetic Terminologies in Application

Understanding how specific combinations lead to visible traits.

ConceptDefinition
HomozygousSame alleles (e.g., BB or bb)
HeterozygousDifferent alleles (e.g., Bb)
AllelesVariants of the same gene
Genetically Modified Organism (GMO)Organism with altered genetic material
Restriction EnzymesProteins used to cut DNA at specific sequences

Chromosomal Abnormalities

Improper chromosome separation can lead to disorders.

Nondisjunction

  • Failure of chromosomes to separate properly during meiosis.
  • Results in gametes with extra or missing chromosomes.
ConditionChromosomal CauseEffects
Down SyndromeTrisomy 21Intellectual disability, facial features
Turner SyndromeMonosomy X (45,X)Short stature, infertility
Klinefelter SyndromeXXY (47 chromosomes)Male with feminine traits, infertility

Karyotype

A karyotype is a visual representation of all chromosomes in a cell.

  • Shows chromosome pairs arranged by size.
  • Used to detect chromosomal abnormalities.
  • Essential in prenatal diagnosis.

Genetic Cross Problem Example

A red-flowered plant (Rr) is crossed with a white-flowered plant (rr).

Rr
rRrrr
rRrrr
  • Genotype: 2 Rr : 2 rr
  • Phenotype: 50% Red : 50% White

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Applied Genetics

Genes can be modified using biotechnology.

  • GMO: Genetically modified organisms are engineered for traits like pest resistance or drought tolerance.
  • Restriction Enzymes: Used to cut genes at specific sites for insertion or removal.
  • Genetic Engineering: Process of modifying DNA to introduce desired traits.

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