bio test rn brochacho (copy)

🧬 Complex Genetics Vocabulary

Codominance – A condition in which both alleles in a heterozygous organism are fully expressed (e.g. AB blood type).

Incomplete dominance – A form of inheritance where the heterozygous phenotype is a blend between both alleles (e.g. red + white = pink flower).

Multiple alleles – When more than two alleles exist for a trait, even though each individual can only carry two (e.g. blood type alleles: A, B, O).

Sex-Linked traits – Traits carried on the X or Y chromosome, usually the X.

Sex chromosome – The 23rd pair of chromosomes that determines sex (XX = female, XY = male).

Polygenic trait – A trait controlled by two or more genes, often showing a range of phenotypes (e.g. height, skin color).

Carrier – An individual who is heterozygous for a recessive disorder but does not show symptoms.

Pedigree – A diagram used to trace the inheritance of traits through generations.

Recessive genetic disorder – A disorder that appears only when an individual is homozygous recessive.

Dominant genetic disorder – A disorder that appears when an individual has at least one dominant allele.


🧬 Vocabulary You Should Already Know

Dominant allele – The allele that expresses itself over another allele.

Recessive allele – The allele that is masked by a dominant one unless both alleles are recessive.

Homozygous – Having two identical alleles for a gene (AA or aa).

Heterozygous – Having two different alleles for a gene (Aa).

Genotype – The genetic makeup of an organism (e.g., AA, Aa, aa).

Phenotype – The physical expression of the genotype.

Autosome – Any chromosome that is not a sex chromosome.


🧪 Incomplete Dominance & Codominance

(Chap 11, sec 2, p302-303)

Q: How can you tell the inheritance pattern based on the phenotype of a heterozygous individual?
A:

  • Mendelian: One allele is dominant, the other recessive (heterozygote shows dominant trait).

  • Codominance: Both traits are visible.

  • Incomplete dominance: Heterozygote shows a blended trait.


🧬 Sickle Cell Anemia (Codominant Disorder)

Q: What do RBCs look like in people with each genotype?
A:

  • Homozygous normal (SS) – Normal-shaped RBCs.

  • Heterozygous (Ss) – Both normal and sickle-shaped RBCs (codominant).

  • Homozygous sickle (ss) – All RBCs are sickle-shaped.


🩸 Multiple Alleles (Blood Types)

(Chap 11, sec 2, p304)

Q: How many alleles are there for blood type?
A: Three – A, B, O.

Q: Which are codominant and which is recessive?
A: A and B are codominant. O is recessive.

Q: What are the genotypes and phenotypes for blood types?
A:

  • Type A: AA or AO

  • Type B: BB or BO

  • Type AB: AB

  • Type O: OO


🧬 Sex-Linked Traits

(Chap 11, sec 2, p307-308)

Q: What sex chromosomes do females have? Males?
A: Females = XX, Males = XY

Q: Are sex-linked traits usually dominant or recessive?
A: Recessive

Q: Is there an allele for sex-linked traits on the Y chromosome?
A: No, usually only the X chromosome carries the allele.

Q: Why do males get sex-linked traits more often?
A: Males have only one X, so one recessive allele is enough to show the trait.

Q: Is a carrier homozygous or heterozygous?
A: Heterozygous

Q: Can males be carriers for sex-linked traits? Why or why not?
A: No, because they only have one X chromosome. They either have the trait or they don't.

Q: Can males be carriers for autosomal traits?
A: Yes, because autosomes are not sex-linked and both sexes have two copies.

Q: Can females be carriers for sex-linked traits? Autosomal traits?
A: Yes, they can be carriers for both.


🌈 Polygenic Traits & Environmental Influence

(Chap 11, sec 2, p309)

Q: What is a polygenic trait?
A: A trait influenced by multiple genes.

Q: Examples of polygenic traits?
A: Height, skin color, eye color.

Q: How is phenotype determined in polygenic traits?
A: By the additive effect of all the genes involved.

Q: What does "additive" mean in polygenic traits?
A: Each allele adds to the expression of the trait.

Q: Which genotype gives darker skin: AABbCc or aabbCC?
A: AABbCc, because more dominant alleles contribute to more pigment.

Q: What genotype gives mid-tone skin?
A: A mix like AaBbCc.

Q: Environmental influence examples?
A: Sun exposure (skin), nutrition (height), temperature (fur color in animals), chemicals (gene expression).

Q: Can environment change genotype?
A: No, only phenotype can be influenced.


🧬 Pedigrees

(Chap 11, sec 1, p299-301)

Q: Why use pedigrees?
A: To track inheritance of traits through generations.

Q: Symbols?
A: Squares = males, Circles = females. Shaded = has trait. Horizontal line = marriage. Vertical line = offspring.

Q: How to tell a trait is recessive?
A: Trait skips generations; unaffected parents can have affected children.

Q: Can you determine relatedness in a pedigree?
A: Yes—use the layout, generations, and connecting lines.


🧬 Recessive & Dominant Genetic Disorders

(Chap 11, sec 1, p296-298)

Match the disorder to the description:

  • Albinism – Recessive; lack of melanin pigment in skin, hair, eyes.

  • Huntington’s – Dominant; causes progressive brain deterioration, symptoms appear later in life.

  • Galactosemia – Recessive; cannot break down galactose, leads to liver damage and intellectual disability.

  • Tay-Sachs – Recessive; lipid accumulation in brain cells, leads to early death.

  • Cystic Fibrosis – Recessive; thick mucus in lungs and organs, breathing and digestion issues.

  • Achondroplasia – Dominant; a form of dwarfism, affects bone growth.