Chapter 9: Genes and Replication Flashcards

1
Q

What is DNA?

A

A nucleic acid found in nearly all cells of every living organism on Earth

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2
Q

Unique blueprint to individual, except what?

A

Clones (identical, not fraternal twins)

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3
Q

DNA is increasingly used in modern society

A

Paternity tests, criminal investigations, genetic testing and behavior

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4
Q

DNA played a role in

A

Inheritance, growth, and development raised more questions than answer

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5
Q

DNA structures are a

A

Double helix, two strands, connected in a twisting ladder structure

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6
Q

The ladder is composed of

A

Nucleotide units, each containing a sugar molecule, phosphate group, and nitrogen-containing base

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7
Q

Hydrogen bonds form between bases on either side of the ladder in specific pairs

A

1) A (Adenine) and T (Thymine)
2) G (Guanine) and C (Cytosine)
3) Means DNA always has the same number of C’s and G’s, and A’s and T’s
4) Because of this, we only have to know the sequence of 1 side to translate the other
5) One human DNA molecule can have 200 million base pair (double helix allows it to fit in a cell)

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8
Q

DNA does the blueprint for

A

How to build and maintain an organism, kept in a code (sequence) of bases

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9
Q

The entire set of DNA is a

A

Genome

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10
Q

Prokaryotes have

A

Small, circular DNA

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11
Q

Eukaryotes have

A

Longer, linear DNA

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12
Q

Broken into short segments called

A

Chromosomes

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13
Q

The number of chromosomes varies between

A

Species

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14
Q

Humans have 46 chromosomes (23 pairs), and the percentage of shared.

A

Genes

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15
Q

Inside a chromosome: Length varies depending upon

A

Species and particular chromosome

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16
Q

Large chunks are

A

Non-coding, with interspersed genes: sequence of bases that code for a product (proteins and RNA)

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17
Q

Inside a chromosome not necessarily one version of a gene variation are called, what?

A

Alleles

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18
Q

Non-coding portion of DNA is called

A

Junk DNA

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19
Q

Junk DNA can be

A

Small (10% bacteria) or large (98% human) proportion of DNA

20
Q

Junk DNA purpose is unclear

A

1) Found between as well as within genes (introns)
2) Long repeating sequences (nonsense sequences), fragments/duplicates of working genes, non-functional variations

21
Q

Not all genes are expressed equally in

A

Cells DNA in each cell codes for everything (in multicellular organism this could be a problem)

22
Q

Each tissue group only expresses genes necessary for

A

Its functioning (why we don’t have hair on our stomachs, or acid on our scalps)

23
Q

Outward expression of trait is

A

Phenotype

24
Q

Genetic material present is

A

Genotype

25
Q

DNA is copied through

A

DNA replication such as:
1) Semi-conservative process
2) DNA replication
3) Real time replication

26
Q

How do we get from DNA to protein?

A

Transcription and translation

27
Q

Transcription copying the gene sequence to

A

Be exported as mRNA (real time)

28
Q

RNA polymerase (an enzyme) pulls apart a piece of DNA at a

A

Promoter site and untwists a short segment

29
Q

RNA polymerase makes an RNA copy of

A

One strand of DNA putting appropriate base pairs on (no T, instead U (uracil))

30
Q

Terminate RNA polymerase hits a termination sequence stops

A

Building RNA, and drops off

31
Q

In eukaryotes add cap and tail to protect

A

RNA ends and for recognition; remove introns; export mRNA to cytoplasm

32
Q

Translation reading of mRNA to

A

Build proteins

33
Q

Translation occurs in the cytoplasm and requires:

A

1) Free amino acids (AA’s) building blocks
2) Ribosomal subunits (builders)
3) Transfer RNA (translator between mRNA and protein languages)

34
Q

Translation initialize

A

Ribosome recognizes start codon (sequence of 3 AA’s - AUG) on mRNA and attaches (small and large subunits)

35
Q

Translation elongate

A

Find appropriate tRNA to translate; attach AA’s to create a protein

36
Q

Translation terminate

A

Ribosome recognizes stop codon, release protein and detach; mRNA can be reused

37
Q

Mutations are errors or alterations in DNA by

A

Deleterious, neutral and beneficial

38
Q

Two classes of mutations

A

Point and chromosomal mutations

39
Q

Mutation point

A

Changing one base pair by replacement, deletions, or insertions, and can cause major downstream problems

40
Q

Chromosomal mutations

A

Change to the sequence of genes on a chromosome by deletions, duplications, and inversions

41
Q

Causes of Mutations

A

1) Spontaneous
2) Radiation-induced
3) Chemical-induced

42
Q

Spontaneous

A

Translation mistake (DNA has a spellcheck function that fixes most of these)

43
Q

Radiation-induced

A

High energy can break apart DNA, increasing errors

44
Q

Chemical-induced

A

Mutagens: react with DNA to increase the rates of mutation

45
Q

Results of Mutations: Wrong genetic code =

A

Bad protein equals to problem

46
Q

Misspelled gene leads to

A

Malfunctioning enzyme (can’t do its job)

47
Q

Mutations often will have

A

One good copy and one bad copy and still function