Biology Unit 2 - Codes

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DNA stands for…

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Includes DNA function, chromatin and chromosomes, gene function, karyotypes, and abnomalities

58 Terms

1

DNA stands for…

deoxyribonucleic acid

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2

In eukaryotes, the DNA is located in…

the nucleus, organelles, chloroplasts, and mitochondria

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3

DNA floats freely in…

prokaryotes

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4

DNA "talks" with the rest of the cell using…

messenger RNA/mRNA (other types of RNA used by DNA are involved in protein synthesis and regulation).

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5

Nitrogenous bases are…

adenine, guanine, thymine, and cytosine

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6

List the Purines (Double carbon-nitrogen ring):

Adenine and Guanine

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7

List the Pyrimidines (Single carbon-nitrogen ring):

Thymine (DNA only) and Cytosine

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8

What are the (Nitrogenous) Base pairing rules?

A pairs with T and G pairs with C

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9

How do DNA strands run?

They run opposite of each other in a double helix (anti-parallel)

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10

Nucleotides (DNA monomers) are made up of…

a 5-carbon sugar, a phosphate base, and one of 4 nitrogenous bases (A, C, T, G)

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11

The 3' end of a nucleotide needs which functional group to have a full valence shell (be stable)?

OH

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12

Where is the 5’ end of a nucleotide?

It is bonded outside the ring and attached to the phosphate group.

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13

Does DNA do anything on its own?

No - it’s the recipe book for the genes (recipes)

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14

Polymerization is…

the creation of molecular chains from smaller units. The chain is called the polymer and the subunits are called monomers

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15

Dehydration synthesis is…

a special type of polymerization that takes two monomers with the functional groups H and OH respectively, bonds the two together, and releases H2O. (A+B = A-B and H2O)

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16

Hydrolysis is…

the reverse of DHS: the breakdown of the water to break the polymer chain.

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17

Chromatin is…

DNA wrapped around histones (a type of protein) and the form DNA usually takes before mitosis or meiosis.

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18

Chromosomes are both…

a long, tightly-packed strand of chromatin or two of these packages

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19

In a chromosome, the singular chromosome is the same as the other and comes from the same parent. We call these single chromosomes…

sister chromatids

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20

Two chromosomes (that are doubled and joined at the centromere) are homologous when…

they have the same genes but come from different parents

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21

The ends of the chromosomes are called…

telomeres

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22

The centromere is…

the center of the point where two sister chromatids are joined. It keeps chromosomes (one chromatid) aligned during cell division.

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23

Nucleosomes are…

DNA wrapped around histones not joined with linker DNA

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24

Chromosomes (two chromatids) that have their centromere near the center and equal-sized p and q arms are called…

Metacentric chromosomes

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25

Chromosomes (two chromatids) that have their centromere closer to one side and a p arm just a little shorter than the q arm are called…

Submetacentric chromosomes

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26

Chromosomes (two chromatids) that have their centromere nearest to one side, a short p arm, and a long q arm are called…

Acrocentric chromosomes

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27

Chromosomes (two chromatids) that have their centromere at the end of the chromosome and just a q arm (p arm so short - not real)

Telocentric chromosomes

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28

Scientists indicate the location of a gene using…

the chromosome number and the arm of the chromosome (E.g. - 17p12 is the 12 location on the 17th chromosome's p arm)

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29

Genes used two program functional products called…

RNA and protein

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30

We can't sequence DNA from a protien because…

the proteins are only programed with exons (missing base introns sequence).

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31

Chromosomes’ (chromatids) two types of areas are…

heterochromatin and euchromatin

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32

Heterochromatin is…

tightly wrapped, and genes here can't be accessed (silent)

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33

Euchromatin is…

less tightly wrapped, and genes can be accessed here. (active)

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34

The genome is….

an organism’s complete set of DNA: exons + introns, functional groups (regulatory sequences), junk DNA (DNA with no clear function)

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35

Sequencing is…

The process of determining the order of the nucleotides (bases, AGCT) in DNA.

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36

The first non-bacterial genome to be sequenced was…

yeast (Saccharomyces cerevisiae)

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37

Exons are…

coding DNA segments for amino acid sequences of proteins found in both prokaryotes/eukaryotes whose sequences are highly conserved (retained in product)

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38

Introns are…

DNA segments that are non-coding, serve as the base between to exons, found only in eukaryotes (?), and sequences are less conserved (not retained in product)

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39

Non Coding DNA is…

DNA composed of introns that doesn’t code for proteins but is important for controlling gene activity, accounts for 99% of the human genome, and undergoes transcription to synthesize most RNA types (excluding mRNAs).

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40

Coding DNA is…

DNA composed of exons that codes for proteins (that have structural, functional and regulatory importance), accounts for 1% of the human genome, and undergoes transcription to synthesize mRNA.

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41

Humans have around ____ bill. base pairs (A, C, T, G), up to __ coding genes (many base pair sets), and __ proteins

3, 25,000, 100-150,000

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42

Do we have more proteins than genes?

yes

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43

Scientists use model organisms to…

run tests on genes shared with humans to preform research

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44

Phenotypes are…

the observable traits associated with a gene

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45

Phenotypic plasticity describes…

the ability of a phenotype to change based on its environment and a gene’s ability to turn on and off

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46

How can we control genes?

By controlling the rate of transcription, RNA processed, or mRNA sent out

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47

A typical karyotype has…

46 chromosomes (two chromatids joined together near mitosis/meiosis)

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48

To create a karyotype, geneticists use _________ dye to create a zebra-like pattern: the heterochromatin is dyed _____ and the euchromatin _____.

Giemsa, black, stays white

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49

Geneticitst pair chromosomes by…

length and chromatin markings

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50

Aneuploidies are…

karyotype abnormalities when a person is missing or has too many chromosomes.

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51

Trisomy describes…

a karyotype that has one too many chromosomes.

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52

Monosomy describes….

a karyotype that has one chromosome too few.

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53

A Monosomy is worse than a trisomy because…

the genetic information is missing. Always results in the death of a fetus/infant.

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54

Terminal deletion is….

the breakage of one end of a chromosome/ the deletion of nucleotides from the terminal end of a DNA molecule

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55

Write the proper notation for a male karyotype with 46 chromosomes.

(Normal) 46 XY

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56

Write the proper notation for a female karyotype with 45 chromosomes (missing a sex chromosome).

Monosomy 45 X0

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57

Write the proper notation for a male karyotype with 47 chromosomes (additional 21 chromosome)

Trisomy 47 XY +21

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58

The sex chromosomes are ____ and _____. Females typically have ___ and males typically have _____.

XX, XY, XX, XY

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