4 Flashcards

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1
Q

James Watson and Francis Crick

A

Credited with discovering the structure of DNA in1953

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2
Q

Describe the structure of DNA

A

1) DNA is located in the nuclues of eukaryotic cells ( or nucleoid region of prokaryotic cells
2) DNA is a double -stranded helix that looks like a twisted ladder. It contains
- The nitrogenous bases
A ( adenine)
G ( guanine)
T ( thymine), and C ( cytosine) that make up the rungs ( steps) of the “ladder.”
( A always pairs with T; G always pairs with C) these pairs are held together by hydrogen bonds.
- A sugar phosphate backbone

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3
Q

Semiconservative Replication

A

how DNA replicates itself. “ Old” strands are used as the template for making “ new” strand of DNA.

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4
Q

Accuracy of DNA replication

A

On average there are about 140 million bas pairs per chromsome

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5
Q

DNA polymerase

A

” proofreads” the DNA strand checking for mismatched pairs. Most, but not all, mismatches are repaired. After “ proofreading”, the error rate is only about on per 10 billion base pairs.

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6
Q

DNA ligase

A

seals the nick or crack left in the sugar-phosphate backbone after the mismatched base (s) are excised and replaced with the correct bases.

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7
Q

One gene-one polypeptide hypothesis

A

One gene codes for the production of one specific polypeptide ( protein,enzyme, horomone).

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8
Q

Structure of RNA

A
  • single-stranded
  • found in nucleus and cytoplasm
    -contains A,G,C, and U (uracil)
    uracil substitutes for thymine
    -contains ribose sugar
    -relatively small molecule
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9
Q

Structure of DNA

A

-Double stranded
-found in nucleus
- contains A,G,C, and T
-contains deoxyribose sugar
-very large molequle

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10
Q

messegner RNA

A

copies genetic “ recipe” from DNA in the nuclues and carries the “ recipe” out into the cytoplasm

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11
Q

What is Transcription and where does it occur

A

synthesis of mRNA using DNA template ( occues in the nuclues)

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12
Q

Describe the process of Transcription

A

1) chemical message sent to the chromosome with the gene that produces a certain polypeptide
2) DNA unzips to expose the gene
3) mRNA is built as complementary nucleotides pair up with bases on the DNA strand
4) once mRNA is built, it leaves the gene and moves out into the cytoplasm; DNA zips up again

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13
Q

What is translation and where does it occur?

A

production of a polypeptide from the genetic meddagr carried by mRNA ( occurs in cytoplams)

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14
Q

Descripe the process of translation

A

1) mRNA associates with ribosomes in the cytoplasm
2) the genetic message is read 3 bases at a time ( 3 bases = one codon)
3) transfer RNA brings an amino acid to the mRNA-rRNA complex; the anticodon on tRNA pairs up with the codon on mRNA
4) a second tRNA brings an amino acid and holds it in place until a peptide bond forms between the two amino acids
5) the first tRNA leaves the complex, the rRNA (ribosome) moves down the mRNA by one codon, and the process continues until the polypeptide is completed.

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15
Q

Codon

A

A sequence of 3 nucleotide bases on mRNA that codes for a signle amino acid ( or stop signal) Of the 64 codons in the gentic code, 61 specify amino acids and 3 specify “ STOP”

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16
Q

Anticodon

A

A sequence of 3 nucleotide bases on tRNA that have the complimentary sequence of codons on mRNA

17
Q

Triplet Code

A

This refers to the genetic code of mRNA codons that each consist of three nucleotide bases.

18
Q

The genetic code is degenerate or redundant what does this mean?

A

Some amino acids are specified by more than one codon, BUT each codon specifies one amino acid ( or a “stop” signal). Redundancy is good because it allows some mutations to “ slip through the cracks” and the correct amino acid is specified anyway.

19
Q

What is meant by the universe salinity of the genetic code

A

The genetic code is a universal code in that most organisms that we know of use this code. That is why we can splice genes from one organism into another, and the recipient organism can express those forgein genes.

20
Q

Gene mutation

A

A change in the DNA sequence of a gene. Mutations can be passed to the next generation only if they occur in the eggs or sperm.

21
Q

Frameshift Mutation

A

Involves an addition or deletion of one or more nucleotide bases. The result is a shift in the “ reading frame” of mRNA. The consequences are not as bad if the addition or deletion is a multiple of 3. If the mutation exist in DNA, mRNA will copy the error each time, resulting in a faulty gene product. Sometimes, mRNA will make an error in copying even though the DNA is correct. This results in a a bad batch of mRNA. Hopefully, next time the mRNA will copy correctly.

22
Q

Point mutation

A

The subsistution of one nucleotide for another. The result is that the incorrect amino acid may be inserted into the protein chain. This depends upon where the point mutation occurs. If it is present in the third position of the codon, then the correct amino acid may be inserted anyway.

23
Q

Mechanisms protecting against gene mutation

A

1)Semiconservative replication
2) base pairing rules
3) DNA polymerase
4) having new mRNAs produced each time a protein product is needed

24
Q

Mutagen

A

any substance or agent that would cause a mutation or change int eh DNA sequence Ex. Radiation, chemicals in tobacco, pollutants in air and water

25
Q

What is the significance of mutations?

A

-Mutations are raw material for evolution (change).
-Most mutations are harmful.
-Some are neutral
- A few may be helpful for survival.

26
Q

Define Gene

A

The unit of heredity located on chromosomes

27
Q

Define Gene expression

A

occurs when the polypeptide product for which the given gene code is

28
Q

What types of controls can effect gene expression?

A

1) cell type
2) cell function
3) chemical conditions within cell
4) outside signals ( i.e. horomones)

29
Q

What is Lyonization?

A

the phenomenon in female mammals where one of the two X chromosomes is inactivated. The inactivated X becomes a Barr body. The same X will be inactivated in all cells from that particular cell line. Female mammals that are heterozygous for alleles on the X chromosomes are mosaic or “ patchwork” for the traits, with some cells expressing the dominant trait and other cells expressing the recessive trait.

30
Q

Define Recombinant DNA and define genetic engineering

A

Both involve the manipulation and transfer of genes from one organism to another or the production of a DNA molecule by combining DNA from different sources.

31
Q

What is the Polymerase Chain Reaction ( PCR)

A

A fast and efficient way to amplify ( make many, many copies) DNA from a small sample obtained from a crime scene or fragment of an organism.

32
Q

How is Polymerase Chain Reaction imprortant?

A

very important especially if only a very small quantity of DNA is recovered many copies can be made for experimentation, finger-printing, and the like.

33
Q

Restriction Fragment Length Polymorphism

A

These are fragments or segments of DNA obtained by using restriction enzymes to cut DNA in precise places. These fragments are then used to make a DNA fingerprint for identification purposes.

34
Q

Examples of Genetic Engineering

A

Plants: frost-resistance, pest-resistance, plants that “ glow” in the dark, plants that can produce biodegradable plastic beads
Animals: transgenic mice that can serve as models for human disease,production of transplantable organs, pigs that produce human hemoglobin
Bacteria: oil-eating bacteria that can leach metal out of low-grade ore, bacteria that can produce
human insulin

35
Q

What is Human Genome Prodject? What was the goal of this prodject?

A

goal was to sequence all of the human chromosomes

36
Q

What is Nuclear Transplantation?

A

involves placing a nucleus from a donor cell into another (recipient) cell. An egg cell has its nucleus removed and then a donor nucleus is inserted. After the egg cell is allowed to go through multiple cell divisions to become an early multicellular embryo, the embryo will be implanted in a surrogate mother where it will develop into a clone of the nucleus donor.

37
Q

Gene Therapy

A

Goal is to replace a faulty gene with the proper gene

38
Q
A