Title | Chapter 6 &7 Meiosis and Sexual Reproductions |
---|---|
Author | Akiba Miller |
Course | Life Science |
Institution | Florida Atlantic University |
Pages | 7 |
File Size | 160.3 KB |
File Type | |
Total Downloads | 32 |
Total Views | 192 |
These notes cover Week 4 Life Science notes in Chapters 6 and 7: Meiosis and Sexual Reproduction....
Chapter 6 &7: Meiosis and Sexual Reproductions ❖ Gene= A sequence of DNA Note: -
Genes provide instructions for making proteins.
-
Two copies of each chromosome (and each gene) in diploid organisms.
-
Homologous chromosomes are one from each parent passed to offspring.
❖ Humans are diploid organisms -
Have two copies of genes found on homologous chromosomes
-
Have some function but DNA sequence may differ
-
MAy have two different alleles of the same gene
Remember: Males is XY, Females is XX ❖ Genotype: Is the particular genetic or allele makeup of an individual (Your genetic makeup). Examples: F=Blue eyes; f=green eyes -
FF=Blue eyed dominant
-
FF=Blue eyed dominant
-
Ff=green-eyed recessive
❖ Phenotype: Is the observable or measurable features of an individual (What you look like). Examples: Blue eyes+ brown hair or brown hair+green eyes or Black hair and Blue eyes Sexual Reproduction ❖ Is the combination of maternal (mother) and paternal (father) -
Are joined together during fertilization
-
Determines the genotype and contributes to the phenotype
❖ Requires special sex cells: sperm, egg -
Sperm comes from Males
-
Eggs come from Females
❖ Gametes: Are reproductive cells that carry one copy of each chromosome Ex: Haploid ❖ Meiosis: Is the special cell division needed to reduce from diploid to haploid -
Meiosis generates genetically unique haploid gametes.
-
Haploid sperm fertilizes a haploid egg resulting in a diploid zygote.
-
Zygotes divide by mitosis into an embryo. Meiosis (two separate divisions)
Meiosis I ➢ Separates homologous chromosomes ➢ Each daughter cell is haploid ➢ Each chromosome still has 2 sister chromatids Meiosis II ➢ Separates sister chromatids ➢ 4 haploid daughter cells are created ➢ Develop into egg or sperm Meiosis and Genetic Diversity ➢ No 2 gametes are Identical due to Recombination and Independent Assortment. ➢ Recombination: When maternal and paternal chromosomes pair and physically exchange DNA segments.
➢ Independent Assortment: Are alleles of different genes are distributed independently of one another. Examples: capital=dominant and lowercase=recessive A=blue eyes D=black hair E=brown eyes d=brown hair e=brown eyes ADe= Blue eyes, black hair, and brown eyes aDE=black hair and brown eyes ade=brown hair and brown eyes Disorders in Chromosome Number ❖ Nondisjunction: Homologous chromosomes fail to separate in Meiosis I or sister chromatids don’t separate in Meiosis II. ❖ Monosomy; fetal development fails (except single X, Turner Syndrome) ❖ Trisomy (extra chromosome) can survive (13,15,18,21,, or 22) 21 Down Syndrome ❖ XXY Kleinfeller syndrome ❖ XO Turner Syndrome ❖ If an egg cell with an extra X chromosome (XX) is fertilized by a sperm cell with one Y chromosome, the resulting child will have Kleinfelter syndrome Key Words
-
Down syndrome= Trisonomy 21
-
Edward’s syndrome= Trisonomy 18
-
Patau syndrome=Trisonomy 13
-
Cri du chat- syndrome= 5p minus syndrome (partial deletion of the short arm of chromosome 5)
-
Wolf-Hirschhorn syndrome= Deletion 4p syndrome
-
Jacobsen syndrome= 11q Deletion disorder
The Inheritance of Traits ❖ The Human life cycle: Growth and reproduction of an individual ❖ Adults produce gametes by meiosis ❖ Gametes (sperm and egg) fuse during fertilization to form single-celled zygotes ❖ Continued cell divisions form the embryo ❖ Genes: Segments of DNA that code for proteins -
Prokaryotes- single, circular chromosomes
-
Eukaryotes-linear chromosomes
Remember: Human cells have 46 chromosomes. Different Alleles ^ Mistakes in copying DNA (mutations) produce different versions of genes. ❖ Homologous pairs: Are equivalent chromosomes; pairs contain one chromosome received from each parent. Note: The parent cell has two complete copies of the manual. Unique Offspring ❖ Segregation in Meiosis: homologous chromosomes separate from each other into
different gametes. -
Gamete gets just one copy of each page manual.
❖ Independent Assortment: Homologous move into gametes, randomly and independently of other chromosomes. -
Due to random alignment during Metaphase I
-
Due to Independent Assortment, the instructions in one sperm cell are a unique combination of pages.
Genetic Diversity ➢ About 8 million different combinations of chromosomes are possible. Note: Random Fertilization produces more diversity: 8 mil x 8 mil=64 trillion possibilities Genotype: recessive and Dominant ❖ Heterozygous: two different alleles (Aa) ❖ Homozygous: two identical alleles -
Homozygous dominant (AA)
-
Homozygous recessive (aa)
❖ Punnett Square: A diagram to determine the probabilities of offspring having particular genotypes. -
Based on the genotype of parents
-
Matches up all possible gametes
For example:
➢ Father is tall and the mother is tall. ➢ But, both parents have a recessive allele for being short. ➢ Hence why both parents have the alleles Tt. ➢ There is a 25% chance that their child comes out short and a 75% chance that the child comes out TALL. Cystic Fibrosis ❖ It is a genetic disease. ❖ Caused by a single gene mutation -
Changes in the nucleotide sequence of DNA
-
Creates a new mutant allele
❖ The allele of the CTFR gene Cystic Fibrosis transmembrane regulator gene ❖ During Cystic Fibrosis, your lungs are clogged up with mucus. ❖ Cystic Fibrosis is most common in European descent. ❖ CFTR moves ions in and out of cells ❖ People with normal phenotypes can still pass CF alleles to offspring. ❖ People with CF alleles can have children that do not come out with the disease.
Note: Cystic Fibrosis (CF) is caused by a recessive allele. -
An allele that affects phenotype only of the organism has two copies of that allele
-
Hidden by a normal or DOMINANT allele
Remember: recessive alleles are lower-cased (aa)(a) and DOMINANT alleles are upper-cased (AA)(A) ❖ Huntington’s disease is a DOMINANT human genetic disease....