SCIENCE LESSON 3 - DNA Flashcards

(61 cards)

1
Q

Are packed in bundles of these
chromosomes, is a distinct of the DNA
responsible for an inherited trait

A

GENES

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2
Q

Are coded instructions for
everything that must happen in the
body, including how an individual
functions and how a person look

A

GENES

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3
Q

Are organic compounds that function as storage of genetic information, which is transmitted from 1 generation to the next in all living organisms

A

Nucleic acids (polynucleotides)

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4
Q

2 TYPES OF NUCLEIC ACIDS

A

DNA
RNA

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5
Q
  • double helix of
    repeating nucleotides
A

DNA

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6
Q
  • sugar (deoxyribose)
  • nitrogeneous bases
    purines (A & G)
    pyrimidines (T & C)
A

DNA

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7
Q
  • carry complex
    information for longer
    period of time, more
    stable
A

DNA

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8
Q
  • helps carry out the
    blueprint’s guidelines
  • able to perform a variety
    of functions, more
    diverse
A

RNA

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9
Q

DNA

A

Deoxyribonucleic acid

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10
Q

Are composed of many
nucleotides linked together in a
long chain

A

Nucleic acids (polynucleotides)

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11
Q

3 components of each nucleotide:

A

a. five-carbon sugar (pentose)
b. phosphate group
c. nitrogenous base

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12
Q

DNA Complementary base pairs, Base pairing for Replication

A

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

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13
Q

Base pairing for Transcription

A

Guanine (G)-Cytosine (C)
Thymine (T)-Adenine (A)
Adenine (A)-Uracil (U)

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14
Q

RNA Complementary base pairs, Base pairing for Translation

A

Adenine (A)-Uracil (U)
Guanine (G)-Cytosine (C)

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15
Q

RNA

A

Ribonucleic Acid

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16
Q

“The
central dogma of molecular genetics.”

A

The DNA, the RNA, and the proteins

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17
Q

RNA 3 processes involve

A
  1. Replication
  2. Transcription
  3. Translation/Protein synthesis
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18
Q

Composition of RNA

A

a. pentose (C5) sugar called ribose
b. phosphate group
c. Nitrogenous base

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19
Q

3 Types of RNA

A
  1. messenger RNA (mRNA)
  2. transfer RNA (tRNA)
  3. ribosomal RNA (rRNA)
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20
Q

Template to create protein, basis to create protein

A

mRNA

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21
Q

Matches amino acids to mRNA to create protein

A

tRNA

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22
Q

Replication

A

DNA to DNA

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23
Q

Ensure all body cells carry the same
genetic material and copied exactly the
instructions

A

Replication

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24
Q

Happens before cell division - new cells
required exact copy of the parent cell’s DNA

A

Replication

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25
3 steps of DNA Replication (Enzymes)
1. UNWINDING ( Helicase, Primase) 2. BASE PAIRING ( Polymerase ) 3. JOINING ( Ligate )
26
First step of replication, opens the DNA
Helicase
27
Serves as primer that separates DNA
Primase
28
Creates a partner for each helix of the DNA after separation
Polymerase
29
Where the partners of each helix are bein set up
3' and 5' (' means prime)
30
Seals up the replicated helix to stop the pairing
Ligate
31
Process of replication because one of the complementing strands is conserved in daughter DNA
Semiconservative replication
32
Transcription
DNA to RNA
33
Making working copies of the genes. DNA only sends copies of blueprints t o RNA, it i s RNA’ s job to make blueprint copies
Transcription
34
Involves the synthesis of a single strand of nucleotides of mRNA using one DNA strand as template
Transcription
35
Translation
RNA to Protein
36
Involves using the mRNA as template to determine the sequence of tRNA, which in turn determine the sequence of amino acids
Translation
37
Is the process involved in genetic information is used to create amino acids and the corresponding proteins
Translation
38
RNA Transcription steps
1) Unzips between its base pairs. 2) RNA Polymerase 3) Pairing (C-G, A-U) 4) mRNA to Cytoplasm
39
The three-base code in the mRNA
Codon
40
In the tRNA, read and translate the message by pairing up an equivalent three-letter code to the codons of the mRNA
Anticodon
41
Changes in the chromosome of organisms that are inheritable and are permanent
MUTATION
42
May also involved a change in the structure of chromosomes or in DNA sequence, can happen spontaneously or can be caused by mutagens or mutagenic agents
MUTATION
43
Mutations based on aneuploids
1. Klinefelter Syndrome 2. Turner Syndrome 3. Metafemale 4. Down Syndrome or trisomy 21
44
This can cause mutations
Mutagens/ Mutagenic Agents
45
Syndrome (mostly seen in men) that shows an abnormally long arms and legs, and abnormal formation of body hairs
Klinefelter Syndrome
46
Syndrome where the 23rd pair of chromosomes is missing an x chromosomes, showing the characteristics of shortness in height, low hairline, widely spaced nipples, and shortened metacarpal, small fingernails, brown spots, no menstruation, and etc.
Turner Syndrome
47
Syndrome that has 3 x sex chromosomes
Metafemale
48
Syndrome that has an uneven 21st pair of chromosomes
Down Syndrome or trisomy 21
49
Mutations based on chromosome structure
- Deletion - Duplication - Inversion - Insertion - Translocation
50
Mutations based on Nucleotide Sequence
- Point mutation or Microlesion ( Deletion and Insertion on nucleotide pair ) - Frameshift mutation ( Deletion and Insertion on DNA ) - Transverse mutation ( change of a purine to a pyrimidine )
51
Control the production of the skin pigment melanin
Tyrosinase
52
Substitution of nucleotide G by another nucleotide A in the codon CGG (arginine) to CAG (glutamine) brought changes in the protein enzyme tyrosinase
ALBINISM
53
The substitution mutation causes a glutamic acid in the protein to be changed to a valine amino acid. - Valine is hydrophobic. Blood cells immediately reflect this change, becoming shriveled and sickle-shaped
Sickle Cell Anemia
54
Is an alteration of the nucleotide sequence of the DNA that makes up a gene. Ex, Hemophilia
Sex cells mutation
55
Mutation in the somatic cells, will not passed along to the next offspring as it occurs in non-reproductive cells
Somatic mutation
56
Genetic disorder characterized by the progressive deterioration of nerve cells in the brain and spinal cord
TAY-SACHS DISEASE OR HEXOSAMINIDASE
57
Autosomal metabolic disorder that results from mutations in a gene located on chromosome 12 for the protein PAH, high level of phenylaline hydroxylase damage neurons in the brain
Phenylketonuria (PKU)
58
Are hereditary genetic disorders where blood- clotting ability is impared due to the mutations of genes found in X chromosome
HEMOPHILIA A & B
59
Disorder that results from the abnormal transport of chloride and sodium across an epithelium caused by mutations in the gene CFTR in chromosome 7
CYSTIC FIBROSIS (CF)
60
A genetic disorder characterized by deletion of certain portion of chromosome 5
CRI-DU-CHAT SYNDROME (CAT’S CRY SYNDROME)
61
A recessive x-linked disease characterized by degeneration of muscle cells, this mutation is due to dystrophin gene located in X chromosome
DUCHENNE MUSCULAR DYSTROPHY (DMD)