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BIOL 1101 Test 3

QuestionAnswer
What three molecules compose a DNA nucleotide? phosphate, sugar, bases
Which two parts of the nucleotide connect to form the backbone of the DNA molecule? sugar and phosphate
What type of chemical bond will hold the nucleotides together? covalent
Are these bonds relatively strong or relatively weak? strong
Why might it be advantageous for the backbone of each DNA strand to be held together by this type of bond? ( covalent) to stay intact for replication
Which component of each nucleotide forms the rungs that link the two DNA strands together? the base
Explain why it is important that hydrogen bonds are weak and covalent bonds are strong. Covalent bonds keep the strand intact for structure and replication. Hydrogen bonds are weaker, allowing for DNA to split.
Chromosomes shorten and become distinct units. Sister chromatids are visible. Prophase
Cytoplasm divides. Cytokinesis
DNA replication occurs. S phase
Final preparation for division is happening. G2
Identical sets of chromosomes reach each pole. telophase
In animal cells, the cell membrane pinches in to separate the cell into two daughter cells. Cytokinesis
In plant cells, a new cell wall forms to divide the cell into two daughter cells. Cytokinesis
Microtubule fibers begin to form at opposite ends of the cell. prophase
Microtubule spindle fibers attach to the centromeres of the sister chromatids metaphase
Nuclear membrane begins to disassemble prophase
Nuclear membrane begins to reassemble around each set of chromosomes telophase
Replicated chromosomes align at the equator of the cell metaphase
Sister chromatids move to opposite ends of the cell anaphase
Spindle fibers disassemble telophase
Spindle fibers shorten, pulling the sister chromatids apart anaphase
The cell enlarges and produces more cytoplasm and new organelles G1
Chromosomes are loosely gathered- not as visible as distinct units Interphase
Number of chromosomes per cell at the start of mitosis 46
Number of chromosomes per cell at the end of mitosis 46
Number of cells formed from one parent cell 2
Diploid number for this organism 23
Three reasons why cells divide Body growth, body tissue renews itself, replaces damaged cells
4 stages, produces 2 diploid daughter cells, chromosome number remains the same Mitosis
8 stages, produces 4 daughter cells, chromosome number is cut in half in each daughter cell Meiosis
Interphase Cell grows and makes a copy of its DNA Preparation for cell division G1, S, G2 phases
G1 phase cell grows, makes extra cytoplasm, copies organelles
S phase the cell synthesizes a complete copy of the DNA in its nucleus duplicates centrosomes centrosomes help separate DNA during M phase
G2 phase cell grows more makes proteins and organelles reorganizes its contents in preparation for mitosis G2 phase ends when mitosis begins
Mitosis Cell divides its copied DNA and cytoplasm to make new cells
Cytokinesis The cytoplasm of the cell is split in two, making two new cells Cytokinesis usually begins just as mitosis ends
Prophase chromosomes begin to coil up Mitotic spindle begins to form Nucleolus disappears
Metaphase chromosomes align in the middle of the cell
Anaphase fibers called microtubules shorten, separating sister chromatids, moves towards the opposite ends of the cell
Telophase daughter cell nuclei are formed cell is almost done dividing starts to establish its normal structures
3 types of conventional cancer treatments surgery, chemo, radiation therapy
Surgery can remove cancerous tissue most effective for solid tumors that are detected early ineffective for widespread cancers
chemotherapy uses toxic chemicals to kill rapidly dividing cells can affect cancer cells that are spread throughout the body side affects are severe
Radiation Therapy uses high energy ionizing radiation to kill targeted cells kills cells by damaging the DNA in cells side effects are severe
Benign tumor non cancerous tumor
malignant tumor cancerous tumor with cells that spread throughout the body
metastasis the spread of cancer cells
number of daughter cells after mitosis two, exact copies of the original cell
Apoptosis the death of cells that occurs in multicellular organisms removes cells during development
Cancer disease of unregulated cell division
centromere the region of a chromosome to which the microtubules of the spindle attach during cell division
sister chromatids identical copies formed by the DNA replication of a chromosome, with both copies joined together by a common centromere.
Proto-oncogene normally promote cell division and differentiation when mutated, they become oncogenes, genes that cause cancer
Tumor suppressor gene normally pause cell division, repair DNA, or initiate cell death can be mutated to become inactivated
Cystic Fibrosis genetic disease caused by a single gene mutation recessive
diploid organisms two copies of every chromosome
homologous chromosomes pair of chromosomes that contain the same genes
genotype the particular genetic or allele makeup of an individual
phenotype observable or measurable features of an individual
Meiosis I separates homologous chromosomes instead of sister chromatids each daughter cell is haploid each chromosome still has two sister chromatids
Meiosis II separates sister chromatids four haploid daughter cells develop into egg or sperm
recombination when maternal and paternal chromosomes pair and physically exchange DNA segments
Independent assortment alleles of different genes are distributed independently of one another
Heterozygote two different alleles (Aa) phenotype is normal individual is a carrier
Homozygote two identical alleles (AA)
How many chromosomes in humans? 46
How many alleles would we carry for a single trait? two alleles
How does the organization of chromosomes , genes, and their alleles contribute to human traits? genes are physically passed down from parents to offspring
Number of daughter cells after meiosis four
Punnett Square a diagram to determine the probabilities of offspring having particular genotypes
what determines biological sex? sex hormones produced by gonads ovaries for females, tested for males
Humans have _____ pairs of chromosomes 23
Hemophilia blood clotting disorder
x-linked trait a phenotype that is determined by the allele on an x chromosome
Pedigree visual representation of the occurence of phenotypes across generations
Incomplete dominance a form of inheritance in which heterozygotes have a phenotype that is intermediate between homozygous dominant and recessive
Codominance an inheritence pattern that explains compatibility of blood types
polygenic a single trait determined by the interaction between alleles of more than one gene
nondisjunction when chromosomes separate unequally
SRY gene necessary for male sex determination in mammals
Anueploidy the condition of having an abnormal number of chromosomes in a haploid set
Karyotype an individual's complete set of chromosomes
Multifactorial inheritance when more than one factor causes a trait or health problem
Polygenic inheritance implies a character or phentypic trait, which is regulated by more than one gene
MRSA infectious bacteria, spreads by skin to skin contact
Binary Fission one parental cell divides into two daughter cells causes changes in DNA
Natural Selection differential survival and reproduction in response to the environment
Directional Selection predominant phenotype shifts in a particular direction
Stablilizing selection phenotype of population settles near middle of range
Diversifying selection phenotype of population is at both extremes of range
When should we use antibiotics? when treating certain infections caused by bacteria
How do bacteria reproduce? Binary Fission
Created by: mykala222
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