Quiz on Meiosis and Karyotypes
Describe the number and organization of human chromosomes in a typical somatic cell. Distinguish between autosomes and sex chromosomes. (8.11 and links below)
Somatic Cell: 46 chromosomes (23 pairs)
They are condensed enough to be viewed with a microscope and arranged into matching pairs
Autosomes: chromosomes other than sex chromosomes (44 of them in humans) are organized with a twin that resembles it in length, centromere position, and staining pattern.
Sex Chromosomes: they determine an individual’s sex and are always in the 23rd chromosome spot; human females have a homologous pair of X chromosomes (XX), but males have one X and one Y which are partly homologous.
Distinguish between somatic cells and gametes and between diploid cells and haploid cells. (8.12)
Somatic Cells: most animals and plants contain pairs of homologous chromosomes (diploid = 2n)
Ex. for humans the diploid number is 46 (2n=46)
Gametes: egg and sperm cells each have a single set of chromosomes (haploid = n)
Ex. for humans the haploid number is 23 (n=23)
Explain why sexual reproduction requires meiosis. (8.13)
It is is required to maintain a constant number of chromosomes in each species from one generation to the next
List the phases of meiosis I and meiosis II and describe the events characteristic of each phase. Recognize the phases of meiosis from diagrams and micrographs. (8.13)
Meiosis I
Prophase I - homologous chromosomes form tetrads, nonsister chromatids of each homologous pair of chromosomes exchange segments (crossing over), the chromosomes condense, the nuclear membrane disintegrates, centrioles move to opposite poles
Metaphase I - homologous pairs line up at the metaphase plate, spindles are attached to the centromeres
Anaphase I - homologous chromosomes separate through the shortening of spindle fibers attached to the centromere and lengthening to separate the poles
Telophase I and Cytokinesis - chromosomes decondense, nuclear membrane reforms around each set of chrosomes, the cytoplasm divides splitting each cell into 2 cells
RESULTS OF MEIOSIS I = 2 Haploid Cells
Meiosis II (essentially the same as mitosis but starts with a haploid cell))
Prophase II - the chromosomes condense, the nuclear membrane disintegrates, centrioles move to opposite poles
Metaphase II - individual chromosomes line up at the metaphase plate, spindles are attached to the centromeres
Anaphase II - sister chromatids separate and become individual chromosomes through the the shortening of spindle fibers attached to the centromere and lengthening to separate the poles
Telophase II and Cytokinesis - chromosomes decondense, nuclear membrane reforms around each set of chrosomes, the cytoplasm divides splitting each cell into 2 cells
RESULTS OF MEIOSIS II = 4 Haploid Gametes
Describe the similarities and differences between mitosis and meiosis. Explain how the result of meiosis differs from the result of mitosis. (8.14)
Similarities
Prophase
Nuclear envelope breaks down
Centrioles move to opposite poles
Chromosomes condense
Metaphase
Spindle has formed (chromosomes are attached)
Anaphase
Spindle fibers shorten (some lengthen to separate poles)
Telophase
Nuclear membrane reforms around each set of chromosomes
Chromosomes decondense
Cytokinesis
Cytoplasm divides splitting each cell into 2 cells
Differences
Prophase - each duplicated chromosome remains separate
Prophase I - homologous chromosomes form tetrads and cross over
Metaphase - duplicated chromosomes line up singly
Metaphase I - duplicated homologous chromosomes line up in pairs
Anaphase - sister chromatids separate
Anaphase I - homologous chromosomes separate
Others:
Mitosis involves one division of the nucleus and cytoplasm while meiosis involves two divisions.
Mitosis starts with a diploid cell, meiosis II starts with haploid cells
Mitosis produces 2 daughter cells, meiosis produces 4 daughter cells
Explain how independent orientation of chromosomes at metaphase I, random fertilization, and crossing over contribute to genetic variation in sexually reproducing organisms. (8.15-8.17)
Independent orientation: Chromosome pairs line up randomly in meiosis, creating different combos of mom’s and dad’s genes.
Crossing over: Chromosomes swap pieces, mixing genes and making each chromosome unique.
Random fertilization: Any sperm can meet any egg, making each baby genetically different
Define nondisjunction, explain how it can occur, and describe what can result (8.18).
Nondisjunction is when chromosomes don’t separate properly during meiosis.
It can happen in meiosis I (homologous chromosomes fail to separate) or meiosis II (sister chromatids fail to separate).
This can result in gametes with too many or too few chromosomes, leading to disorders like Down syndrome (extra chromosome 21).
Explain how and why karyotyping is performed (8.19).
Karyotyping is a process where scientists take a picture of a person's chromosomes, arrange them in pairs, and check for abnormalities.
It’s done by collecting cells (like from blood), stopping them during cell division, and staining the chromosomes so they can be seen under a microscope.
Karyotyping is used to diagnose genetic disorders (like Down syndrome) and to check for extra, missing, or damaged chromosomes.
Describe the main types of chromosomal alterations (8.23).
Deletion - a segment of a chromosome is removed
Duplication - a segment of a chromosome is copied and inserted into the homologous chromosome
Inversion - a segment of a chromosome is removed and then reinserted opposite to its original orientation
Reciprocal translocation - segments of two nonhomologous chromosomes swap locations with each other