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64 Cards in this Set
- Front
- Back
What does degenerate mean? |
Some codons encode for the same amino acid |
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Where does translation occur? |
Within the ribosome |
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How many amino acids and codons are there? |
20 Amino Acids and 64 potential codons |
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3 steps of translation |
initiation, elongation, termination |
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Initiation |
translation begins with the start codon (AUG) methionine |
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Elongation |
ribosome uses tRNA anticodons to match codons and amino acids to grow the chain |
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Termination |
The RNA polymerase falls off and translation ends at stop codon (UAG, UAA, UGA) |
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What is the large subunit of the ribosome made up of? |
49 proteins and 3 RNA molecules |
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What is the small subunit of the ribosome made up of? |
33 proteins and 1 RNA molecule |
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3 binding sites for tRNA? |
Esite, Psite, Asite |
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How does translation terminate? |
The release factor binds to the A site |
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What must happen after protein synthesis? |
Proteins must fold into their 3D shape |
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What do proteins do? |
Catalyze chemical reactions and control the transport of nutrients |
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What keeps a protein in its 3D shape? |
Non-covalent bonds like ionic, hydrogen and van der waals AND hydrophobic interactions |
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What is primary structure? |
Amino Acids linked one by one |
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What is secondary structure? |
Amino Acids chains fold to produce alpha helixes and pleated sheets |
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What is tertiary structure? |
A combination of secondary structures that form a 3D structure |
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What is Quaternary Structure? |
Stable interaction of proteins to form a complex |
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How are misfolded proteins destroyed? |
Ubiquitin tags the error proteins and transport it to a proteosome to be degraded |
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What is a Prion? |
A protein folding disorder |
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Example of prions |
Scrapies, Bovine Spongiform Encephaly and variant creutzfeldt-jakob disease |
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What does the endocrine system do? |
produce hormones that travel great distances to their target cells |
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What does the exocrine system do? |
produce hormones that are secreted directly into ducts leading directly to their target organs |
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Gene Expression is controlled by: |
Transcription Factors, Mutations, Number of Gene Copies and Histone Code |
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Removing a methyl group will turn |
transcription on |
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Adding a phosphate or acetyl group will turn |
transcription on |
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1.5% of the human genome encodes ________ |
proteins |
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How is it that proteins outnumber genes? |
alternative splicing and cutting of proteins translated from a single gene |
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What else does the human genome encode for? |
viral dna, noncoding RNA, introns, promoters, repeats |
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What is the difference between a mutation and a polymorphism? |
A mutation occurs in less than 1% of the population, a polymorphism occurs in more than 1% of the population. |
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What is a somatic mutation? |
A mutation that occurs in the body cells and isn't transmitted to offspring |
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What is a germ line mutation? |
mutation that has a possibility of being transmitted to an offspring |
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Examples of mutation diseases? |
Sickle cell, early onset Alzheimer's, and Ehler Danlos syndrome |
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What happens in Sickle Cell? |
A Valine is produced instead of a Glutamic Acid, resulting in abnormal aggregation of hemoglobin molecules |
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What is Thalessemia? |
An excess of alpha hemoglobin and a too few beta hemoglobin which leads to heart, liver and endocrine gland damage |
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What is Ehler Danlos Syndrome? |
"The stretchy man" A mutation prevents procollagen chains from being cut |
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What are spontaneous mutations? |
new mutations not caused by exposure to known mutagens and may be due to errors in DNA replication |
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Mutation Rate Formula |
number of cases/2 * (number of individuals in population) |
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What are mutational hot spots? |
Short repetitive sequences, palindromes, duplications of larger regions |
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What is the Ames Test |
in vitro test to test the mutagenicity of a substance |
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What is a point mutation? |
A change of one single nucleotide |
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What is a missense mutation |
Changes the amino acid |
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What is a nonsense mutation |
A mutation that inserts a stop codon |
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What is a splice site mutation |
mutation that alters the site where introns are normally removed |
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Insertions or deletions NOT in a multiple of 3 lead to: |
frameshift mutations |
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What is a pseudogene? |
A DNA sequence similar to a gene but isn't translated (May be transcribed tho) |
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What is a copy number variant? |
Sequences in more than one place in a genome |
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Silent mutations |
do not affect the amino acid encoded |
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The system for fixing mismatched DNA favors the |
newly synthesized strand |
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Types of DNA damage: |
mismatches, deamination, depurination, breaks and crosslinking |
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What protein monitors DNA repair? |
P 53 |
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Trichothiodystrophy cause and effect? |
cause: oxidative damage effect: faulty nucleotide or base excision repair |
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Colon cancer ? |
defect in mismatch repair |
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Xeroderma Pigmentosa cause and effect? |
cause: malfunction of excision repair effect: must avoid UV light |
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Ataxia Telangiectasis? |
defect in cell cycle checkpoint kinase-> cancer |
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Cell Specialization depends on: |
proteins expressed, amounts of proteins, timing of proteins, how different cell types respond |
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What is Biotechnology? |
The use of cells or biological molecules for specific applications |
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What is the morphagen model? |
Growth factors moved between cells |
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What is the Sequential Induction Model? |
Event takes place in one area and is passed to another area |
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What is Competence? |
The ability of cells to respond to external cutes |
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What is Commitment? |
intrinsic aspect of a cell that makes it follow a particular developmental path regardless of enviornment |
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What is PCR? |
process that replicates and amplifies the amount of DNA sequence in a tube |
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3 major steps of PCR? |
1. denaturation 2. annealing 3. extension |
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What is recombinant DNA? |
the combination of DNA from two different sources (gene cloning) |