1/34
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced |
---|
No study sessions yet.
Mitosis
Ensures that every body cell has 23 pairs of chromosomes; occurs during growth and repair of damaged cells
Meiosis
Involved in formation of gametes; produces haploid cells with 23 chromosomes
Importance of Meiosis
Reduces chromosome number and shuffles genes to produce genetically different gametes
Homologous Chromosomes
Same size
Diploid Cells (Humans)
Have 22 pairs of autosomes and 1 pair of sex chromosomes (46 total)
Sex Chromosomes
Males are XY; females are XX
Alleles
Different versions of the same gene that may code for different protein formsMeiosis I
Meiosis II
Sister chromatids separate into two cells each
Synapsis
Homologous chromosomes pair and line up side by side in meiosis I
Tetrad
Association of four chromatids (two homologous chromosomes with two chromatids each)
Crossing Over
Exchange of genetic material between non-sister chromatids
Genetic Recombination
Shuffling of alleles during crossing over to create diversity
Chiasma
Point where crossing over has occurred
Recombined Alleles
New genetic combinations formed during meiosis II when chromatids separate
Independent Assortment
Random separation of homologous chromosome pairs at metaphase I
Prophase I
Tetrads form; crossing over occurs; nuclear envelope fragments
Metaphase I
Tetrads align at spindle equator; either homologue can face either pole
Anaphase I
Homologues separate; dyads move to poles
Telophase I
Daughter nuclei are haploid
Interkinesis
Rest period between meiosis I and II; DNA replication does not occur
Prophase II
Chromosomes condense; nuclear envelope fragments
Metaphase II
Dyads align at spindle equator
Anaphase II
Sister chromatids separate into daughter chromosomes
Telophase II
Four haploid genetically different daughter cells are formed
Mitosis vs Meiosis II
Both separate sister chromatids; both produce daughter cells with the same number of chromosomes as the parent
Nondisjunction
Failure of homologues (meiosis I) or sister chromatids (meiosis II) to separate
Down Syndrome (Trisomy 21)
Three copies of chromosome 21
Sex Chromosome Errors
Can result in XXX
Triplo-X (XXX)
Female with three X chromosomes; mild symptoms
Klinefelter Syndrome (XXY)
Male with extra X; symptoms include infertility and tall stature
Jacobs Syndrome (XYY)
Male with extra Y; often taller than average; usually no unusual features
Turner Syndrome (XO)
Female missing an X; short stature
Chromosomal Rearrangement
Can delete or duplicate genes
Inversion
Gene order is flipped
Translocation
Two non-homologous chromosomes exchange parts