The exam includes:
Multiple-choice questions
True-False questions (correct the false)
Fill-in-the-blank questions
Types of Questions:
60-75% of the test is MC/TF/F
25-40% will be short answer
Potential to interpret diagrams or figures
Sex Chromosome: Chromosomes that dictate sex (X and Y).
Autosome: Non-sex chromosomes that determine other traits.
Homologous Chromosomes (Homologs): Chromosomes that have the same genes at the same loci but may have different alleles.
Genome: The complete set of genetic material in an organism.
Ploidy: The number of sets of chromosomes in a cell.
Haploid: A cell with one set of chromosomes (n).
Diploid: A cell with two sets of chromosomes (2n).
Karyotype: A display of the chromosome pairs of a cell.
Gene: A unit of heredity.
Allele: Different versions of a gene.
Haploid Number: The number of chromosomes in a haploid cell.
Fertilization: Union of sperm and egg to form a zygote.
Synapsis: Pairing of homologous chromosomes during meiosis.
Bivalent: A pair of homologous chromosomes during meiosis.
Sister vs. Non-sister Chromatids: Sister chromatids are identical copies; non-sister chromatids are homologs.
Chiasmata: Points of crossover between homologous chromosomes.
Crossing Over: Exchange of genetic material between homologous chromosomes.
Principle of Independent Assortment: Genes are inherited independently of one another.
Genetic Recombination: Creation of new gene combinations.
Nondisjunction: Failure of chromosomes to separate properly during cell division.
Aneuploidy: Abnormal number of chromosomes (e.g., trisomy, monosomy).
Gamete: Mature reproductive cell.
Trisomy: Three copies of a chromosome instead of the normal two.
Monosomy: One copy of a chromosome instead of the normal two.
DNA is packaged into structures called chromosomes.
Meiosis: Process of cell division that reduces the chromosome number by half to produce haploid gametes.
Fertilization: Restores diploid condition by combining two haploid gametes.
Sister chromatids: identical duplicates of a chromosome.
Non-sister chromatids: from homologous chromosomes (maternal vs. paternal).
Ability to identify organism's ploidy based on karyotype.
Overview: Sequences include Meiosis I (reduces ploidy) and Meiosis II (similar to mitosis).
DNA Replication: Occurs before Meiosis I.
Meiosis I Products: Haploid cells (n) with duplicated chromosomes (result of division).
Meiosis II Products: Haploid cells (n) with single chromosomes (similar to mitosis).
Involves processes of meiosis (gametes), fertilization (zygote), and mitosis (growth).
Occurs during prophase I with specific terminology like bivalent and chiasmata involved.
Result: Increases genetic variation.
Homologous pairs align during metaphase I (unlike mitosis where sister chromatids align).
Relates to independent assortment and the genetic diversity it provides.
Introduces genetic variation into populations.
Down Syndrome as case study for nondisjunction in meiosis II.
Asexual reproduction leads to genetically identical offspring; sexual reproduction produces diversity.
Diverse populations fare better in variable conditions.
Understand sex chromosome combinations typical for males (XY) and females (XX) in mammals.
Analyze karyotypes for evidence of sex and aneuploidy cases.
Sex Determination: SRY gene leads to male development; absence leads to female.
Draw distinctions among:
Haploid cell with one chromatid
Haploid cell with duplicated chromatid
Diploid cell with one chromatid
Diploid cell with duplicated chromatid
In mammals, the sperm determines the sex of the offspring.
Typical crossover patterns occur mostly at the ends of sex chromosomes.
Conditions leading to XY female or XX male development.
Phenotype: Observable traits.
Genotype: Genetic makeup.
Dominant vs. recessive traits, homozygous vs. heterozygous alleles.
Pure-breeding: Individuals with homozygous genotypes.
Hybrid: Offspring resulting from a cross between different genotypes.
Mendelian Concepts: Monohybrid, reciprocal, and dihybrid crosses, testcrosses, linkage, and different inheritance patterns.
Blending inheritance suggests traits mix, but Mendelian patterns reveal discrete inheritance.
Peas had clear traits, were easy to cultivate, and allowed controlled crosses.
Pure-breeding traits consistently shown in the F1 generation.
Dominance explains which traits appear; segregation explains allele separation during gamete formation.
Use squares to predict offspring ratios and infer parent genotypes from offspring traits.
Genes assort independently during gamete formation, leading to varied offspring combinations.
Traits located on sex chromosomes can show different inheritance patterns.
Linked genes tend to be inherited together unless crossing over occurs.
Traits may show more than two alleles; dominance can be complete, co-dominant, or incomplete.
External conditions can affect expression of traits.
Traits influenced by multiple genes with continuous variation.
Pedigrees illustrate inheritance patterns through generations, particularly for human traits.
Exam 6: Learning Objectives for Chapters 13 and 14