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67 Cards in this Set

  • Front
  • Back

What is RNA and DNA made of?

phosphate group, 5 carbon sugar and nitrogenous base

what are the types of nitrogenous base and their pairs?

pyrimidines: thymine and cytosine


purine: adenine and guanine


thymine pairs with adenine


guanine pairs with cytosine

what is the shape of DNA

anti- parallel, and a double stranded helix

what are the 3 levels of condensation of DNA

1: packaging DNA into nucleosomes


2: supercoiling


3: attachment of fibres to a protein scaffold

explain the first level of condensation

-starts as 2nm and goes to 11nm


-146 nucleotide pairs wrap around an octamer of histones


-wrapped around 8 histone proteins and anchored by 9th histone (H1)

whats a complete nulceosome in condenstation?

8 histones, 146 base pairs and histone H1

what can happen to linker DNA?

linker DNA can be susceptible to digestion by endonuclease

what happens in the second level of condensation?

-condenses to 11nm to 30nm


-the nucleosomes wrap around each other



what happens in the third level of condensation?

30nm fibre is attached at many positions to a protein scaffold

what are the two proteins used in the third level of condensation and what do they do?

cohesin: proteins that hold the two arms together


codensin: condenses the 30nm of chromatin within one sister chromosome

what are the three parts of the chromosomes?

p arm: refers to the short arm


q arm: refers to the long arm


centromere: point of attachment of chromosomes microtubules in miotic spindle

what do telomeres do?

protect the end of the chromosomes, prevent fusion and facilitate replications

where does mitosis occur?



in all non-germ cells

what are the 5 phases of the cell cycle and what happens?

G1: growth, cellular metabolism


S: DNA replication


G2: prep for mitosis


M: mitosis


interphase: time between successive mitosises

what is a sister chromatid?

make up a chromosome and are identical

haploid vs diploid vs DNA content (in terms of n and c)

haploid: 'n' and 'c' amounts of DNA, one chromosome


diploid: 2'n' and 2'c', one unique chromosome from mom and dad

what are the 6 steps in mitosis

interphase, prophase, metaphase, anaphase, telophase and cytokinesis

interphase:

-chromosomes duplicate to produce sister chromatid


-sister chromatid are homologs

prophase:

-duplicated chromosomes condense


-nulceolus disappears


-nuclear membrane starts to breakdown



metaphase:

chromosomes migrate to the middle

anaphase:

sister chromatids pull apart and move to opposite poles of the cell


-cohesin breaks down

telophase:

chromsomes decondense and new nuclear membrane forms


-new daughter cells are 2c and 2n

cytokinesis

membrane forms between daughter cells

where does meiosis occur and what does it produce?

-occurs in germ cells


-results in 4 haploid genetically distinct cells

what are the steps in meiosis?

meiosis I: prophase 1, metaphase 1, anaphase 1, telopahse 1


meiosis 2: prophase 2, metaphase 2, anaphase 2, telophase 2

what are the steps in prophase 1:

-leptonema: sister chromatids condense


-zygonema: homologous coromosomes begin to pair


-pachynema: crossing over occurs here


-diplonema: homologous chromosomes seperate at the chiasmata

explain crossing over

breakage of chromatids and the exchage of broken pieces between homologous chromosomes

what happens in metaphase 1 and 2?

-1: paired chromosomes align in the middle


-2: chromosomes align in the middle



what happens in anaphase 1 and 2?

-1: homologous chromosomes disjoin andmove to opposite poles


-2: sister chromatids disjoin and go to opposite poles

what happens in telophase 1 and 2?

-1: new nuclei begin to form (n;2c)


-2: haploid cells are seperated by cytoplasmic membranes (n;c)

whats the difference between a locus and an allele?

locus: fixed position on a chromosome


allele: alternate form of a gene (Aa)

what is a genotype?

a genotype refers to the allelic combination

what is a phenotype?

the physical appearance caused by the allelic combination

what is the difference between homozygous and and heterozygous?

homozygous: both alleles and identical; either dominant or recessive


heterozygous: two alleles are different

what are the three designations when doing crosses?

P: parent generation


F1: parents offspring


F2: parents grand-offspring

what is the genotypic and phenotypic ratio for a monohybrid cross?

1,2:1 and 3:1

what is Mendel's principle of inheritance?

in heterozygous, dominant allele masks the recessive

Mendel's principle of segregation?

in a heterozygous, two alleles segregate from each other during formation of gametes

Mendel's principle of independent assortment?

alleles on different pairs of chromosomes assort independently from one another

pseudoautosomal:

found in the terminal region, genes that don't follow the X or Y linked pattern

What's the difference between heterozygous and hemizygous?

heterozygous: recessive allele is masked by dominant allele (XX)


hemizygous: recessive allele would manifest because there is nothing to mask it (XY)

what happens to the second X chromosomes in women?

X- chromosome condenses into darkly staining matter called Barr Body

what is a spontaneous mutations?

error during DNA synthesis when are isoforms of the bases occur

what are the alternate forms of the bases?

keto-thymine: enol form


amino-cytosine: imino form


amino-adenine: imino form


keto- guanine: enol form

what happens in the isoforms of the bases?

adenine and cytosine bound and guanine and thymine bound

what are the hot spots for spontaneous mutations?

simple repeats, symmetrical repeats and palindromes

what are the two types of chemical mutagens?

-mutagenic only to replicating DNA(base analogues, acridine dye)


-mutagenic to both replicating and non-replicating DNA

what can cause chemical mutations?

UV rays can cause thymines to mutate into thymine dimers

what are transposable elements?

virus puts segments into DNA which causes early stoppage

what are the type of single base (point) mutations?

silent: no effect to resulting amino acid


nonsense: results in early stop


missense: changes one amino acid

what are the types of frameshift mutations?

insertion: insertion of base pair, shifts coding to the right


deletion: deletion of base pair, shifts coding to the left

expanding genes

expanding genes show increased severity and severity earlier in life by generation

mutations that affect coding regions

changes the protein to a non-functional form


-premature truncation


-changes protein folding


-changes post- translational modification

mutations that affect non-coding regions

prevent or reduce transcription or translation

what is incomplete dominance?

one allele is partially or incompletely dominant over the other

what is codominance?

heterozygotes express both phenotypes of both the homozygotes


-blood type (AB)

what is the allelic series?

a hierarchy displayed by the dominance of mutations within themselves

what is a test cross?

if you want to find the genotype of something, cross is with a homozygous being

complementation test?

cross two mutations together to see if a new mutation forms

what are the 3 stages in transcription?

initiation, elongation and post-translational modifications

what happens in initiation (transcription)?

RNA polymerase binds ta the DNA upstream of gene being copied (promoter)


-rich in A's and T's

what happens in elongation (transcription)?

-once bound to the promoter, the polymerase builds the mRNA single strand in 5prime to 3prime


-only one DNA is copied, called the template strand


-as polymerase passes, double helix reforms



what happens during post- translational modifications?

-capping and tailing: 50- 250 adenines added to the 3prime, 5prime cap of 7 guanine to initiate translation


-introns removed: introns are removed by spliceosomes as they don't code for amino acids



what are the 3 stages of translation?

initiation, elongation and termination

what happens in initiation (translation)?

-large and small ribosome subunits associate with mRNA


-tRNA molecule containing amino acid Met joins to small ribosomal unit at the P site


-complex binds to the 5prime cap of mRNA and large ribosomal subunit binds to complete ribosome

what happens in elongation (translation)?

-tRNA is bound at the P site


-next tRNA w/ anticodon and amino acid bind to A site


-met is cleared and forms polypeptide bind with amino acid on A site tRNA


-ribosomes move along the mRNA to the next codon and empty tRNA moves to E site and is released


-tRNA move from A site to P site and new tRNA brings amino acid to A site

what happens in termination (translation)?

-A site arrives at stop codon


-polypeptide is released