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If short hair(L) is dominant to long hair(l), animals LL and Ll have the same
phenotypes
a ribozyme is
an RNA capable of catalyzing reactions similar to the action of protein enzymes
an RNA capable of catalyzing reactions similar to the action of protein enzymes
*extension occurs at the 5' end *both strands are replicated *the lagging strand is synthesized using RNA primers *takes place in the S phase
the condition occurring when an organism has 2n+1 chromosome composition is known as
trisomy
the region in a tRNA that bonds with mRNA during translation is the
anticodon
the portions of a gene that are transcribed but not translated are called
introns
the place where RNA polymerase first associates with DNA so that transcription can begin is called the __and is located__ of the transcribed region
promoter, upstream
at the start of translation the initiator tRNA is base paired with the start codon at __ in the ribosome.
the P site (peptidyl site)
An X-linked carrier is a
heterozygous female
what are the contributions of James Watson and Francis Crick?
*established the double stranded nature of DNA *established the principle of base pairing based on . Franklins data *explained how DNA's structure permitted it to be replicated *proposed the concept of the double helix
replication of DNA in Eukaryotes
is semi-conservative
pattern baldness is a trait that is referred to as sex..
linked
translation ends when a stop codon is at the __ site, allowing a __ to bind there.
A, release factor
suppose the 1st part of a new polypeptide chain being produced in a eukaryotic cell does not have a signal peptide. Where would you expect translation to occur?
cytoplasm only
if short hair (L) is dominant to long hair (l) then what fraction of the offspring produced by a cross of Llxll will be homozygous?
none
a gene that produces multiple effects is call
a pleitropic gene
during meiosis II
sister chromotids of each chromosome are separated from each other
DNA replication occurs
between the gap phases of interphase
which applies to a cell underling mitosis?
the daughter cells have identical genes and these genes are identical to those of the mother cell that produced them
symptoms of phenylketonuria(PKU) may be minimized or suppressed by a diet low in
phenylalanine
the TATA box is a key lemon of the __ of most eukaryotic protein-coding genes
promoter
a women is diagnosed to have the genetic disease known as Huntington's disorder. It is a rare defect caused by an autosomal dominant allele. the chance for nay one of her children to inherit the disease is
one out of two
during elongation stage of transcription
*RNA nucleotides are added to the transcript *the transcript grows in the 5'-->3' direction *RNA polymerase unwinds the DNA *the double helix reforms behind RNA polymerase
DNA and RNA are alike in
*the pentose sugar *all the nitrogenous bases used to assemble the genetic code *The number of strands *their function in genetics
if one parent has type A blood and the other has type B, what types of blood are possible in their children?
A,B,AB,&O
the docking sites on the centromeres are called
kinetochores
males tend to be affected in greater numbers by X linked recessive genetic disorders than are females because
males have only one recessive gene for the disorder
which is an exception to the principle of independent assortment
linkage
examples of post-translational modification
*phosphorylation *glycosylation *attachment to ubiquitin *quartenary structure folding
a polysome is
an mRNA molecule with many ribosomes attached
the process of removing introns from mRNA and putting the remaining eons together occurs together occurs in a complex called the
spliceosome
in what stage of translation doe the peptide bind join 2 amino acids?
elongation
which if the following carries amino acids to ribosomes, where amino acids are linked into the primary structure of a polypeptide
mRNA
when both the dominant and recessive alleles are expressed (such as pink flower color in snapdragons), that trait is called
codominant
the genetic code is made up of units of which consist of how many nucleotides?
3
the form of RNA that carries the code from the DNA to the site where the protein is assembled is called
messenger RNA
the central dogma describes the flow of information of eukaryotic gene expression as
DNA-->RNA-->protein
an autosomal recessive disorder
will appear only in children of parents who both carry the gene
the sex chromosome composition of a person with Klinefelter syndrome is most accurately written as
XXY
aneuploidy would describe all the following except
translocation
crossing over
increases variability in gametes
precursor-mRNA (pre-mRNA) typically exists
only in the nucleus of eukaryotes
which of the following of conditions exhibits codominance?
sickle cell anemia
chromosomes other than those involved in sex determination are known as
autosomes
chromatics that are attached at the centromere are called what kind of chromatids?
sister
how many different kinds of RNA codons are there in eukaryotes?
64
if all the offspring of a test cross are alike and resemble the organism being tested, then that parent is
homozygous dominant
the probability of producing a child who suffers from cystic fibrosis by two parents who are carriers for the autosomal recessive disorder is
25 %
frameshift mutations may involve
addition or deletion of one to several base pairs
centrioles
are responsible for the orientation of the cell division spindle
centrioles
hn RNA
if a parent cell has 16 chromosomes and undergoes meiosis, the resulting cells will have how many chromosomes?
8
meiosis typically results in the production of
4 haploid cells
__ are large protein complexes that degrade __.
proteasomes, proteins
which of the following dominates in the process of transcription?
RNA polymerase
Red green color blindness is an X-linked recessive trait in humans. What is the probability that a color blind woman and a man with normal vision will have a color blind daughter?
0%
which of the following best describes homologous chromosomes
*they may undergo reciprocal exchange of genetic material during meiosis *they have alleles for the same characteristics even though that gene expression may not be the same *they are in pairs, one chromosomes of each pair from the father and one from the mother
all mRNA transcripts begin and end with
AUG and poly A

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