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115 Cards in this Set

  • Front
  • Back

Genome

All the DNA in a cell

Telomeres

Chromosome ends

Somatic cells

non reproductive cells that have 2 sets of chromosomes

Gametes

reproductive cells (sperm and egg) have half as many chromosomes as somatic cells

Mitosis

The division of the nucleus

Cytokinesis

The division of the cytoplasm

Prophase

Replicated chromosomes thicken and shorten. Centrosomes moving outward

Pro-metaphase

Chromosomes continue to thicken. Spindles extend from centrosomes and bind to kinetichore of centromere

Metaphase

Chromosomes are pushed to the midline of cell by spindles

Anaphase

centromere splits, spindles begin to shorten and pull chromosomes apart. Two sister chromatids are now two separate chromosomes

Telophase

Chromosomes are pulled to opposite ends of the cell. Cell is prepared to divide

Mitotic spindle

apparatus of spindles that controls chromosome movement during mitosis

aster

radial array of short microtubules that extends from each centrosome

Genetics

Scientific study of heredity and genetic variation

Heredity

The transmission of traits from one generation to the next

Variation

differences in appearance that offspring show from parents and siblings

Genes

units of heredity made up of segments of DNA

Asexual reproduction

two parents give rise to offspring that have unique combinations of genes inherited from the two parents

Clone

genetically identical individuals from the same parent

Sexual reproduction

two parents give rise to offspring that have unique combinations of genes inherited from the two parents

autosomes

The 22 pairs of chromosomes that do not determine sex

diploid cell

two sets of chromosomes

haploid cell

single set of chromosomes (gamete)

zygote

fertilized egg, has one set of chromosomes from each parent

Meiosis I

results in two haploid daughter cells with replicated chromosomes

Meiosis II

Results in four haploid daughter cells with un replicated chromosomes

synapsis

homologous chromosomes loosely line up, aligned gene by gene

Crossing-over

non-sister chromatids exchange DNA segments

Chiasmata

X-shaped regions where crossing over occurred

Mutations

Changes in an organisms DNA, source of genetic diversity

hybridization

mating two contrasting true breeding variaties

P-generation

true breeding parents

F1 generation

hybrid offspring of the p generation

F2 generation

when F1 generation self-pollinates

alleles

alternate versions of a gene

Law of segregation

states that two alleles for a heritable character separate during gamete formation and end up in different gametes

monohybrids

individuals that are heterozygous for one character

dihybrids

crossing two true breeding parents differing in two characters

Law of independent assortment

each pair of alleles segregates independently of each other pair of alleles during gamete formation

Complete dominance

occurs when phenotypes of the heterozygote and dominant homozygote are identical

Incomplete Dominance

the phenotype of F1 hybrids is somewhere between the phenotypes of the two parental varieties

Codominance

two dominant alleles affect the phenotype in separate distinguishable ways

Quantitative characters

those that vary in the population along a contiunuum

polygentic inheritance

additive effect of two or more genes in a single phenotype

Sex-linked gene

Gene located on either sex chromosome

Barr body

The Inactive X

Linked genes

genes located on the same chromosome that tend to be inherited together

genetic recombination

the production of offspring with combinations of traits differing from either parent

parental types

Offspring with a phenotype matching one of the parental phenotypes

recombinants

Offspring with non-parental phenotypes

Genetic map

an ordered list of the genetic loci along a particular chromosome

Linkage Map

A genetic map of a chromosome based on recombination frequencies

Map units

Distances between genes

non-disjunction

pairs of homologous chromosomes that do not separate normally during meiosis

Aneuploidy

results from the fertilization of gametes in which non disjunction occurred


Polyploidy

condition in which an organism has two complete sets of chromosomes

Inversion

reverses a segment within a chromosome

Translocation

moves a segment from one chromosome to another


Semi-conservative model

Watson and Cricks idea that when a double helix replicates each daughter molecule will have one old strand and one new strand

Origins of replication

where the two DNA strands are separated, opening up a replication bubble

Replication fork

Y-shaped region where new DNA strands are elongating

Helicases

Enzymes that untwist the double helix at replication fork

Topoisomerase

corrects "overwinding" ahead of replication forks by breaking swiveling and re-joining DNA strands

primase

can start an RNA chain from scratch and adds RNA nucleotides one at a time using the parental DNA as a template

DNA polymerases

catalyze the elongation of new DNA at a replication fork

Okazaki Fragments

How the lagging strand is synthesized which are joined together by DNA ligase

DNA polymerase III

synthesizes new DNA by covalently adding nucleotides to the 3' end of a pre existing DNA strand or RNA primer

DNA polymerase I

Removes RNA nucleotides of primer from 5' end and replaces them with DNA nucleotides

mismatch repair

repair enzymes that correct errors in base pairing

nucleotide excision repair

a nuclease cuts out and replaces damaged stretches of DNA

Gene expression

process by which DNA directs protein synthesis, includes transcription and translation

Transcription

the synthesis of RNA under the direction of DNA

Translation

The synthesis of a polypeptide which occurs under the direction of mRNA

Ribosomes

site of translation

primary transcript

initial transcript from any gene

Triplet-code

the flow of information from a gene to protein a series of non-overlapping three nucleotide words

template strand

provides a template for ordering a sequence of nucleotides in an RNA transcript

codons

mRNA triplets read in the 5'-3' direction

RNA polymerase

How RNA synthesis is catalyzed, pries te DNA strands apart and hooks together the RNA nucleotides

Transcription factors

mediate the binding of RNA polymerase and the initiation of transcription

transcription initiation complex

A promoter that contains transcription factors and RNA polymerase II

TATA box

promoter crucial in forming the initiation complex in eukaryotes

introns

non coding regions

exons

usually translated into amino acid sequences

RNA splicing

removes introns and joins eons creating an mRNA molecule with continuous coding sequence

tRNA

How a cell translates an mRNA message into a protein

wobble

allows for some tRNAs to bind to more than one codon

P site

holds the tRNA that carries the growing polypeptide chain

A site

holds the tRNA that carries the next amino acid to be added to the chain

E site

exit site where discharged tRNAs leave the ribosome

polyribosome

A number of ribosomes that can translate into a single mRNA simultaneously

Mutations

changes in the genetic material of a cell or virus

Point mutations

changes in just one base pair of a gene

base pair substitution

replaces one nucleotide and its partner with another pair of nucleotides

missense mutations

still code for an amino acid but may not be the correct one

non sense mutations

changes amino acid codon to a stop codon

frameshift mutation

Insertion or deletion altering the reading frame

operator

Regulatory switch, usually positioned within the promoter

operon

entire stretch of DNA that contains the operator promoter and genes that they control

repressor

How the operon is switched off, blocks RNA polymerase

core-repressor

molecule that cooperates with a repressor protein to switch an operon off

inducer

inactivates the repressor to turn the lac operon on

CAP catobolite activator protein

an activator of transcription subject to control through a stimulatory protein

cyclic AMP

When glucose is scarce, how CAP is activated

histone acetylation

acetyl groups attach to positively charged lysine's in histone tails

genomic imprinting

methylation regulates expression of either the maternal or parental alleles of certain genes at the start of development

alternative RNA splicing

different mRNA molecules produced from the same primary transcript depending on which RNA segments are treated as exons and introns

Proteasomes

giant protein complexes that bind protein molecules and degrade them

miRNA

micro-RNA small single stranded RNA molecules that bind to mRNA

RNAi

Inhibition of gene expression by RNA molecules caused by small interfering RNAs

Transformation

New DNA integrated into the bacterial chromosome

Conjugation

The ability of bacterial cells to exchange DNA through a structure called pili

Transduction

the movement of DNA from one bacterial cell to another by way of bacteriophage

Transposons

Fragments of DNA that have the ability to replicate/jump to other areas of a genome

Hardy Weinburg Equations

Used to determine allele or genotypic frequencies found in a population