Genetic Processes and Principles
Meiosis and Mitosis
Definition and Overview
Meiosis and mitosis are two types of cell division that contribute to genetic diversity and growth.
Comparison of Meiosis and Mitosis
Mitosis is utilized for somatic cells and results in two identical daughter cells.
Meiosis results in four genetically diverse gametes, reducing chromosome number.
Key terminology:
Somatic cells: 46 chromosomes (diploid).
Gametes: 23 chromosomes (haploid).
Genetic Diversity in Meiosis
Characterized as a "shuffling of genes."
Crossovers during Prophase I contribute to diversity by exchanging genetic material between homologous chromosomes.
Independent assortment occurs, allowing for different combinations of alleles to be passed to gametes.
Chromosome Numbers
Start with 92 chromosomes (4n), resulting from DNA replication, and end with 46 (2n) in the first meiotic division leading to gametes with 23 (n).
In mitosis, the amount is doubled from 46 to 92 and then back to 46.
Phases of Cell Division
Mitosis has a longer interphase to ensure precise replication.
Meiosis entails a reduction division for genetic variation.
Probability in Genetics
Difficult Concepts
Students may encounter challenging aspects of probability related to sex-linked disorders and genetic combinations.
Understanding likelihood rather than performing mathematical calculations.
Terminology
Familiarity with terms such as homozygous (AA or aa), heterozygous (Aa), and true breeding is essential.
Dominant traits mask recessive traits in heterozygous combinations.
Genotype and Phenotype
Phenotype: Observable traits (e.g., appearance).
Genotype: Genetic makeup that determines possible traits.
Ratios in offspring, such as 3:1 for dominant to recessive traits, need to be memorized.
Punnett Squares
Useful for visualizing genetic crosses and determining the likelihood of certain genotypes and phenotypes.
Can illustrate ratios based on genotypes of parent plants or animals (e.g., homozygous dominant vs. homozygous recessive).
X-Linked Traits and Disorders
X-Linked Inheritance
Inherit dominant or recessive traits through the X chromosome.
Male children inherit their Y chromosome from their father, while they receive one X chromosome from their mother, affecting the expression of X-linked traits.
Female offspring can be carriers without expressing the disorder.
Transmission of Disorders
A mother who is a carrier (heterozygous) has a 50% chance of passing on the affected allele to a son (who can either express the recessive trait or not).
Male offspring have no chance to inherit a second X from the father and thus will express any X-linked disorder if inherited.
Daughters can inherit the disorder based on the genotype of both parents.
Genetic Mapping
Recombinant DNA and Crossover
Genes far apart on a chromosome are more likely to assort independently due to frequent recombination events during meiosis.
The closer genes are, the lower the probability of recombination, meaning they tend to be inherited together.
Distance on Chromosomes: The unit for mapping distances is generally a 1% probability of recombination reflecting one map unit (centimorgan).
Usage of Chromosomes and Traits
Examples show likelihood ratios (likelihood of color traits, body types) to understand crossing over probabilities.
Karyotypes and Nondisjunction
Karyotype Definition
A karyotype is an organized profile of an individual’s chromosomes, used for identifying chromosomal abnormalities.
Nondisjunction
Failure of chromosomes to separate properly during cell division, leading to an abnormal number of chromosomes in the daughter cells.
Trisomy 21 (Down syndrome) is a common result of nondisjunction during meiosis.
Aging and Trisomy Risks
Older maternal age increases the risk of nondisjunction in gametes because eggs have been in suspension for many years and undergo many divisions.
Additionally, while males produce sperm throughout life, the quality can decline with age as well.
Conclusion
Review Techniques
Emphasize understanding over memorization for tests.
Utilize breeding examples and vocabulary accurately to familiarize with genetic concepts.