BIOL 1100 Unit 04 (Ch 14, 15, 16, 17) Flashcards
(39 cards)
phage
(also, bacteriophage) virus that infects bacteria
DNA monomer
nucleotide that uses deoxyribose
RNA monomer
nucleotide that uses ribose
DNA replication models
3 models (conservative, semi-conservative, and dispersive)
Semi-conservative model (of DNA replication)
DNA replication where the two strands come apart – each acts as a template for synthesis of a new complementary strand.
DNA base pairs
A-T, G-C
RNA base pairs
A-U, G-C
what is the flow of information in the cell
DNA encodes RNA, which in turn encodes protein.
DNA is first transcribed into mRNA.
then mRNA strands are then translated into proteins
Transcription initiation
In transcription: When RNA polymerase binds to a specific region on DNA called the promoter, marking the start point for RNA synthesis (initiates RNA synthesis)
transcription elongation
the stage of transcription where RNA polymerase adds nucleotides to an RNA strand to create a full RNA transcript
(RNA polymerase adds complimentary nucleotides (A, U, C, G) to make the mRNA)
Process:
RNA polymerase moves along the DNA template strand, adding a complementary RNA nucleotide (AUCG) to the 3’ end of the RNA strand for each DNA nucleotide.
Result:
The RNA transcript is almost identical to the DNA coding strand, but with uracil (U) replacing thymine (T) and a slightly different sugar.
transcription termination
final step in the transcription cycle, where the RNA polymerase and the nascent RNA are released from the DNA template
(transcription ends when RNA polymerase transcribes a terminator sequence: The process stops and the mRNA is released)
transcription (what and where)
transcription is the process of copying a gene’s DNA sequence into messenger RNA (mRNA). This process takes place in the nucleus of a cell.
translation (what and where)
translation is the process of using the information in mRNA to produce a protein chain, or polypeptide. This process takes place in the cytoplasm of a cell
codon
three consecutive nucleotides in mRNA that specify the
insertion of an amino acid or
the release of a polypeptide chain during translation
anticodon
three-nucleotide sequence in a tRNA molecule that corresponds to an mRNA codon
mutation
change in the nucleotide sequence of the DNA strands.
base substitution
(also, Missense) type of point mutation; a type of genetic mutation where one nucleotide (base) in a DNA sequence is replaced with another, essentially swapping one “letter” of the genetic code for another at a specific position
(most common nucleotide mutation;
two types, either transitions or transversions.
Transition substitution refers to a purine or pyrimidine being replaced by a base of the same kind; for example, a purine such as adenine may be replaced by the purine guanine.
Transversion substitution refers to a purine being replaced by a pyrimidine, or vice versa; for example, cytosine, a pyrimidine, is replaced by adenine, a purine.
frame shift
a genetic mutation that occurs when a DNA sequence is altered by the insertion or deletion of one or more nucleotides that is not a multiple of three;
(This disrupts the reading frame of the DNA sequence, which is the grouping of codons. drastically altering the reading frame and leading to a completely different amino acid sequence downstream.
Frameshift mutations are generally predicted to trigger more substantial clinical consequences than other types of mutations)
RNA splicing
pre-mRNA is transformed into mature mRNA by removing introns and joining exons together
the process where a newly formed precursor messenger RNA (pre-mRNA) is transformed into a mature mRNA by removing non-coding regions called introns and joining the coding regions, known as exons, together to create a functional protein-coding sequence; essentially, it’s a form of RNA editing that removes unnecessary parts to produce the final message for protein synthesis
Intron
non–protein-coding intervening sequences that are spliced from mRNA during processing; the non-coding segments removed during splicing
A sequence of DNA between exons that is copied into RNA, but is not part of the final mRNA transcript
exon
sequence present in protein-coding mRNA after completion of pre-mRNA splicing; the coding segments that are joined together to form the mature mRNA
how can one gene can code for many different polypeptides?
A single gene can code for multiple polypeptides through a process called “alternative splicing,” where different combinations of exons within the gene are spliced together during RNA processing, resulting in various mRNA molecules that translate into distinct polypeptides with potentially different functions; Splicing different combinations of exon together can lead to the production of a variety of different proteins being produced from a single gene
Signal transduction pathway
the process by which a signal molecule binds to a receptor on the outside of the plasma membrane to initiate a chemical or physical series of molecular events through the inside of the cell; a series of molecular interactions that occur when a signaling molecule binds to its receptor on a cell’s surface. This process activates various intracellular pathways that are involved in cell signaling
What initiates a Signal transduction pathway
a signal molecule binding to a receptor on the outside of the plasma membrane (cell surface)