Biology unit test

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83 Terms

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Gene

Short segment of DNA that controls expression of trait

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Hormones

Proteins critical for transportation

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What makes organism uniques

Order of nitrogen base in DNA

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Double helix

Shape of DNA

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Chromosomes

Coiled DNA inside nucleus carries genetic information for specific set of traits in genes

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DNA stands for

déoxyribonucléic acid

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Somatic cells

Body cells have 46 chromosomes or 23 pairs, diploid have two replicates, made by mitosis

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X and Y chromosomes

Somatic cells 23rd pair but can have different number of x or y détermine sex

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Gamete

Sex cells only found in ovaries or testes, 23 chromosomes haploid means only single copy, meiosis,

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Interphase stages

Growth 1 phase, Synthesis phase, growth 2 phase

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Growth 1 phase

Cell makes new molecules + grows larger, duration of growth varies depending on type + health of cell

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Synthesis stage

Chromatin (uncoiled chromosomes) are duplicated form sister chromatids held together by centromere

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Growth 2 phase

Synthesize more molecules grows larger

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Contact inhibition

‘Normal’ cells stop dividing when coming into contact with like cells

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Chemotherapy

Halt cell division

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Cancer drugs

Damage RNA or DNA induce cell suicide (apoptosis)

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Cell-cycle specific drugs

Kill when dying

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Cell-cycle non-specific drugs

Kill cancer cells resting

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Normal cells affected by chemotherapy

Blood cells, mouth cells, stomach + bowel, hair

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Side effects of chemotherapy

low blood counts, mouth sores, nausea, diarrhea, hair loss

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Mitosis

P: sister chromatids are visible M: line up A: pulled apart T: new nucleus

<p>P: sister chromatids are visible M: line up A: pulled apart T: new nucleus </p>
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DNA

molecules in cell has instructions make other cell parts

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Who made double helix model and when and what was their first mistake and how did they fix it

James Watson and Francis Crick in 1953 thought paired like with like (A with A) but then didnt result in uniform width of DNA molecule, found needed specific pairing

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What does DNA look like

Anti parallel strands that twist around each other

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What unit is DNA made of

Nucleotides, basic unit of nucleic acid

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What are nucleotides made of

Sugar (deoxyribose), phosphate group, one of four nitrogen bases

<p>Sugar (deoxyribose), phosphate group, one of four nitrogen bases</p>
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4 nitrogen bases

Adenine (A), Guanine (G), Cytosine (C), Thymine (T)

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Nitrogen base pairs

Apples in the tree (A to T), Car in the garage (C to G)

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What are the nitrogenous base pairs held together by

Hydrogen bonds, AT have two, CG have three

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Rosalind Franklin DNA discovery

X-ray crystallography found two antiparallel sugar phosphate backbones paired in DNA’s molecule interior

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Karyotype and use

Taken picture of chromosomes used to diagnose disorders

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Allele

Variations on gene

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Homologous chromosomes

Identical chromosomes in length, centromere location and banding pattern, one from each parent, alleles found on same gene of these chromosomes

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How many alleles for hair color gene

4

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<p>double single blue stick from each parent with brown background image from slides</p>

double single blue stick from each parent with brown background image from slides

diploid and unreplicated (single stranded), autosomes and sex chromosomes

Beginning interphase somatic cells

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When are sex chromosomes homologous

Only in females, x chromosome

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Autosomes

First 22 pairs of homologous chromosomes

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<p>Transparent background realistic ish chromosomes grainy pinched in middle</p>

Transparent background realistic ish chromosomes grainy pinched in middle

Double replicated chromosomes, look like x with sister chromatid connected by centromere, somatic cells visible in prophase also starting cells make gametes in ovaries + testes

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<p>White background single sticks from which karyotype is it with black lines in single sticks</p>

White background single sticks from which karyotype is it with black lines in single sticks

Gamete haploid and unreplicated, 23 chromosomes, after fertilization zygote get diploid unreplicated

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What is n

Indicate # chromosome copies in species ie humans n = 23

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How are chromosomes arranged in karyotype

Largest to smallest by size

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gametogenesis

meiosis

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What is the starting and ending cell type in meiosis?

Starts with 1 diploid cell (2n) from either ovaries or testes and ends with 4 haploid daughter cells (n)

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Reduction division

Homologous chromosomes separated make haploid cells

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What happens in Meiosis I

Nuclear membrane dissolves, centrioles, P1: chromosome pairs w/ homologous form tetrad, crossing over happens, M1: still forming tetrad homologous pair chromosome line up tetrad double line A1: pull pair apart reduction division T: nuclear membranes MIGHT cytoplasm divides

<p>Nuclear membrane dissolves, centrioles, P1: chromosome pairs w/ homologous form tetrad, crossing over happens, M1: still forming tetrad homologous pair chromosome line up tetrad double line A1: pull pair apart reduction division T: nuclear membranes MIGHT cytoplasm divides</p>
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Meiosis II

Mitosis but two haploid cells are coordinated nuclear membrane reforms

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Tetrad

homologous chromosomes pair up

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Crossing over

the exchange of genetic material between homologous chromosomes during Prophase I of meiosis like switching shoes

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Is meiosis a cycle

No

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Spermatogenesis

Meiosis form 4 sperm cells

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Oogenesis

Meiosis 1 egg cell 3 polar bodies contribute cytoplasm make one large egg cell

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which one have haploid ending cell which one diploid in mitosis vs meiosis

Haploid meiosis cells, diploid mitosis

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what occurs in zygotes and most body cells

Mitosis

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Part of cell division that produces growth

Mitosis

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Promotes variation among offspring

Meiosis

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Ensures same number of chromosomes between generations

Mitosis

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Sister chromatid

two identical newly replicated chromosomes joined by centromere

<p>two identical newly replicated chromosomes joined by centromere</p>
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Trisonomy

person has three copies of chromosomes (weird)

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genetic variation methods

Independent Assortment, Crossing Over, Non-disjunction Chromosomal Mutations, Structural Chromosomal Mutations, Nucleotide Point Mutations

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Law of Independent Assortment 

when different traits don’t depend on each other to show up

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Non-disjunction chromosomal mutation

Sister chromatids or homologous chromosomes refuse to seperate resulting in n + 1 or n - 1

<p>Sister chromatids or homologous chromosomes refuse to seperate resulting in n + 1 or n - 1 </p>
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Polyploidy

Extra sets of chromosomes

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Structural chromosomal mutation, four main types

Mutation in chromosome structure, deletion, duplication, inversion, translocation

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Nucleotide point mutations

Mistake in DNA replication cause addition, substituition or deletion of nitrogen base pair

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Purebred

Homozygous dominant

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F1

First fillial generation (kids)

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genotype vs phenotype

genetic makeup vs appearance

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test cross

Determine genotype of individual showing dominant trait by making them have babies with a homozygous recessive

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Incomplete dominance 

When dominant allele doesn’t commit and red and white flower make pink flower, but also two alleles are equally dominant

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Codominance

Both alleles dominant shows up at the same time (red and white cow)

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Why focus on x linked genes

Because x chromosome bigger than y has more alleles

<p>Because x chromosome bigger than y has more alleles</p>
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Mendel’s laws of inheritance 

Law of segregation, law of independent assortment, genes located on chromosomes

<p>Law of segregation, law of independent assortment,&nbsp;genes located on chromosomes </p>
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Law of segregation

Ability of chromosomes in meiosis to be pulled apart randomly

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term image

Must be autosomal recessive because two unaffected parents have affected child

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term image

Dominant because two affected have unaffected

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term image

recessive because two unaffected have affected kid then all kids get it

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term image

dominant because two affected parents have unaffected child

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example of trisonomy

Down syndrome

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synthesis of new DNA

another way to just say DNA replication

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precipitate

Two chemicals mix together to form a solid

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translocation

when one homologous chromosome pair’s chromosome does crossing over with another homologous chromosome pair (ex. Chromosome 1 pair crossing over with chromosome 15 pair)

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difference between point mutations and missense mutations 

point have no effect on protein making but missense make non-working protein 

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what number start out in interphase end in mitosis and meiosis

start 4n end mitosis 2n and meiosis n