BIO EK WRONG Flashcards
Gene expression
- involves RNA polymerase binding to the PROMOTOR & catalyzing the sysnthesis of RNA & eventually protein
- pay attention when the passage talks about gene expression, becuase you can connect that DNA will occupy a certain state (such as Z-DNA-passage said gene expression) while mRNA production of CFTR gene on chromosome 7 takes place
rough ER has a similar ionic concentration to what?
-
inter-nuclear membrane enviroment
- the ourter-nuclear memebrane is continuous with endoplasmic reticulum thus it is safe to say that both organelles are enviromentally similar
- cytoplasmic enviroment differs quite a bit from the inside of the nuclear & ER lumens
Cells that would contain Euchromatin?
- a cell with numerous origions of replication
- Euchromatin is UNCOILED at several origions of replication that eukaryotic DNA has, where the enzyme machinery binds to begin replication or transcription
- only dividing cells (i.e., mucus-producing goblet cells, epithelial cells) have a high nuclear concentration of euchromatin
Which cells would have high Heterochromatin?
- neurons & heart muscles
- they are considered permanant & therefore arrested in the G0 phase of the cell cycle, thus are not considered to be transcriptionally active
T/F: viruses have euchromatin?
FALSE, VIRUSES DO NOT HAVE EUCHROMATIN
Southern Blotting
IS USED TO ANALYZE AND NOT AMPLIFY , genetic pattern of interest that may appear in DNA
ELISA
used to locate the presence of antibodies to a particular infection
- it is a primary test for HIV
can mtDNA be considered a unique identifier in forensic sciences?
- NO, becuase the maternal mitochondrial cell line is passed on to every offspring
- mtDNA is only from the maternal cell line
- that same mtDNA is passed on from the mother to every offspring the women bears, thus mtDNA cannot be considered a unique identifier, becuase more than one individual can have the same mtDNA
- in fact, even apparently unrelated individuals might share an unknown maternal relative at some point in the distant past, evidenced by common mtDNA
During the addition of an incoming dNTP nucleotides, a linkage is formed & a pyrophosphate is released. Which of the following describes a type of bond that occurs between two dNTP molecules?
- REPHRASE THE QUESTION: what is the name of the bond that is formed between 2 nucleotides? ANSWER: PHOSPHODIESTER BOND
HIGH YIELD: Which RNA is the smallest and have a cloverleaf shape?
- tRNA

in translation which is responisbile for proofreading activity?
aminoacyl-tRNA synthases
not ribosomes, and not the A sites etc becuase they are located on the ribosomes
replication of the chromosome involves what type of DNA polymerase synthesis
semi-discontinuous
question 157 & 160 about primers!!
Frameshift mutation & inframe mutation
frameshift mutation: occurs when there is an addition of 1 or 2 base pairs
in-frame mutation: is a 3 base pair addition or deletion will cause an in-frame mutation
ribosomes must be “read” the mRNA in the what direction?
5’ to 3’ direction!!
what is the max number of nucleotide of (GCAU)4:
- 4
- write it out and look for AUG, thus it has 4 amino acids
Does meiosis centromeres divide at anaphase I?
no, becuase during anaphase Meiosis I, homologous chromosomes, not centromeres, seperate & migrate to the opposite poes of the cell
Anticipation
in a genetic disease is associated with an earlier onset of symptoms as well as an increase in disease severity with every generation
anticipation is usally seen in autosomal dominant diseases associted with triple repeat exapnsion (huntington’s). The problem is believed to result because triple repeat sequences of increased lenght are unstable during cell division
Heterozygous advantage
- occurs when being a heterozygous carrier of a specific trait is a benefit; for example, individuals that are heterozygous for sickle cell trait are less likely to catch malaria
Penetrance
- is used to explain, the fact that some persons may carry a mutant allele but not show any sign of the disease
post-translational modification
golgi & RER
ionic bonding is stronger than covalent interactions: T/F
true
methylated genes are what type of chromosome
heterochromatin
Barr Body?
-
it is a permanantly inactivated X chromosome that forms a dense stainable nuclear mass
- a normal female with XX inactivates one of her X’s while expressing the other
- she therefore has 1 barr body
- A normal male, who is XY, does not inactivate his only X chromosome, & therefore has no barr bodies
- a male who is XXY would inactivate his one extra X, giving him one Barr Body
- the main rule:
- the number of X chromosomes is always 1 More than the number of Barr bodies
- a person with 2 barr bodies must have 3 X chromosomes
Autosomal Dominant
- a person needs a single copy of the mutant gene to inheit the disease
- traits do not skip generations (called vertical transmission)
- they are usually equal number of affected males & females
- father to son transmission is observed
mutation happens in:
proteins!!! not carbs!
Autosomal recessive