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120 Cards in this Set

  • Front
  • Back
Chromatin
DNA + Proteins
Condenses to prepare for division
Forms thread like chromatin
sister chromatids
have identical DNA, are joined at the centromere
karyotype
a photographic inventory of an individuals chromosomes produced from dividing white blood cells
human karyotype
23 pairs arranged and numbered. 1-22 are autosomes. X & Y are sex chromosomes.
autosomes
homologous chromosomes contains same set of genes
homologous chromosomes
are matched in length centromere position.
gene location
-alocus is the position of a gene, different versions of a gene may be found at the same locus on maternal and paternal chromosomes.
sex chromosomes
X&Y differ in size and genetic composition. Males Have one X and one Y. Females have two X's.
somatic cells
two copies of each chromosomes one from mom & one from dad, called diploid (2N)
Gamentes
only have one copy of each chromosome called haploid (1N)
How many chromosomes have in their somatic cells?
total of 4
How many chromatids are present in the karyotype?
?
How many pairs of chromosomes do humans have in their somatic cells
2 pairs
How many homologous pairs does a female have?
23
How many homologous pairs does a male have?
22
How did we end up with 2 copies (pairs) of each chromosome?
we get one half from mom, one half from dad.
mitosis
produces genetically identical cells
1 each 2N cell - two N daughter cells that are genetically identical.
One N cell - two, One daughter cell that are genetically identical
meioses
Is the process that converts diploid nuclei 2 n To haploid nuclei 1n.
One 2n cell - four, 1n daughter cells that are NOT genetically identical
Meioses only occurs in the sex organs producing gametes.
daughter cells
are gametes (sperm & egg)
fertilization
the union of sperm 1n and egg 1n to form a zygote 2n
zygote
is a diploid cell, it is a fertilized egg that is the beginning stages of a baby.
organism reproduced by two methods
a-sexual,
sexual
a-sexual reproduction
offspring are identical to the original cell or organism, involves inheritance of all genes from one parent.
sexual reproduction
are similar to parents but show variation of traits, involves inheritance of unique sets of genes from two parents
How does cell division perpetuate life?
every cell from a cell,
mitosis,
meiosis,
What happens in Mitosis during cell division?
reproduction of an entire single cell organism.
growth of a multi-cellular organism.
growth of a fertilized egg to an adult.
replacement of cells in an adult.
What happens in Meiosis during cell division?
sperm and egg production.
binary fusion
occurs in prokaryotic cells (dividing in half) two identical cells arise from one.
steps in the process of binary fusion?
a single circular chromosome duplicates and copies begin to separate from each other.
the cells elongate, and the chromosomal copies separate further.
the plasma membrane grows inward to divide the cells.
cell cycle
is an ordered sequence for cell division that consists of two stages,
interface phase, (duplication of cell contents)
mitotic phase, (division)
Interphase
the duplication of cell contents
G1-growth, increase in cytoplasm
S-duplication of chromosomes (S is synthesis of DNA)
G2 - growth, preparation for division
mitotic phase
division
mitosis- division of a nucleus
cytokinesis - division of the cytoplasm
stages of mitosis
prophase
pro-metaphase
metaphase
anaphase
telephase
mitotic spindle
divides the chromosomes
is composed of microtubules
produced by centrosomes, structures the cytoplasm that organizes microtubule arrangement. contains a pair of centrioles in animals.
what changes occur in interphase?
in the cytoplasm, the cytoplasmic contents double. two centrosomes form.
In the nucleus, the chromosomes duplicate during the S phase nucleoli, sites of ribosomes assembly are visible.
What changes occur in prophase?
in the cytoplasm, microtubules begin to emerge from centrosomes, forming the spindle.
in the nucleus chromosomes coil and become compact, nucleolus disappear.
What changes occur in pro-metaphase?
spindle microtubules reach chromosomes where they attach at kinetochores on the centromeres of the sister chromatids.
Move chromosomes to the center of the cell thru the associated protein motors. The nuclear envelope disappears.
What changes occur in metaphase?
spindle is fully formed. chromosomes align at the cell equator. Kinetochores of sister chromatids are facing the opposite poles of the spindle.
what changes occur in anaphase?
sister chromatids separate at the centromeres, daughter chromosomes are moved to the opposite poles of the cell. the cell elongates.
What changes occur in telephase?
cell continues to elongate. the nuclear envelope forms around chromosomes at each pole, establishing daughter nuclei. chromatids uncoil, nucleoli reappear, the spindle disappears.
What changes occur in cytokinesis?
is divided into separate cells.
cytokinesis
in animal cells, a cleavage furrow forms, deepens to separate the contents into two cells.
In plants, a cell plate forms in the middle from vesicles containing cell wall material. the cell plate grows outward to reach the edge, dividing the contents into two cells. each cell has plasma membrane and cell walls.
Cell division
definition -
Results of Cell division
are
compare the types of nuclear division mitosis and meiosis.
?
contrast of the types of cell division of mitosis and meiosis.
?
distinguish between somatic cell and a gamete-forming (germ) cell.
?
distinguish between a-sexual and sexual production.
a-sexual - self reproducing
sexual - half from mom, half from dad
what is the difference between DNA, chromosomes and chromatin?
?
Identify a duplicated chromosome with its sister chromatids and centromere.
?
Describe the events of a cell cycle of a eukaryotic cell including interphase, mitosis, cytokinesis and make a connection between them.
?
Distinguish between the three of interphase, G1, S, G2.
G1 Cell growing, threads link
S synthesis DNA, chromatin are copied and attached at the centromere
G2 - cell grow more, produce enough material to continue on to prophase.
Recognize that different species differ in their chromosome number.
?
Define Haploid and Diploid number of chromosomes and relate it to the two parents of human offspring.
?
State the diploid chromosome number for humans.
?
explain the difference between the human sex chromosomes X&Y and the other chromosome pairs?
?
describe the process of mitosis including its phases, prophase, anaphase and telephase.
?
identify the phases in diagrams and micrographs.
?
compare cytokinesis in plants and in animals mitosis.
?
define homologous chromosomes (homologous) gene, allele, gametes (egg and sperm) fertilization, zygote
?
describe the process of meiosis including its phases (prophase 1, metaphase 1, anaphase 1, telephase 1, prophase 2, metaphase 2, anaphase 2, telephase 2) Identify the phases in diagrams.
?
explain how crossing over and the independent orientation of chromosomes contribute to genetic variation of offspring.
?
identify and explain the characteristics of cancer cells.
?
compare a cancer cell with a normal cell using the example of a normal skin cell with a cancerous skin cell.
?
define tumor,
?
define benign tumor
?
define malignant tumor
?
define cancer
?
define metastasis
?
describe a karyotype and its use
?
explain the following structural changes in chromosomes: duplication, inversion, deletion, translocation.
?
explain how non disjunction causes changes in chromosome number. Use downs syndrome as an example.
?
give example of 6 chromosomal changes in number
?
The monomer unit of DNA and RNA is the nucleotide containing
Nitrogenous base
5-carbon sugar
Phosphate group
DNA and RNA are polymers of
nucleotides
DNA and RNA are polymers called polynucleotides
-a sugar-phosphate backbone is formed by covalent bonding between the phosphate of one ----
nucleotide and the sugar of the next nucleotide
-Nitrogenous bases extend from the sugar-phosphate backbone
DNA is composed of two polynucleotide chains joined together by
hydrogen bonding between bases, twisted into a helical shape
DNA is composed of two polynucleotide chains joined together byhydrogen bonding between bases, twisted into a helical shape
-the sugar phosphate backbone is on the outside
-teh nitrogenous base are perpendicular to the backbone in the interior
-Specific pairs of bases give the helix a uniform shape
-A pairs with T, forming two hydrogen bonds
-G pairs with C, forming three hydrogen bonds
DNA replication follows a
semiconservative model
DNA replication follows asemiconservative model
-the two DNA strands separate
-each strand is used as a pattern to produce a complementary strand, using specific base pairing
-each new DNA helix has one old strand with one new strand
DNA replication begins at the orgins of replication
-DNA unwinds at the origin to produce a bubble
-replication ends when products from the bubbles merge with each other
DNA replication occurs in the 5'-3' direction
-replication is continuous on the 3'-5' template
-replication is discontinuous on the 5'-3' template, forming short segments
Enzymes involved in DNA replication
-DNA polymerases ( adds nucleotides to a growing chain)
-DNA ligase ) joins small fragments into a continuous chain)
The DNA genotype is expredded as proteins, which provide the molecular bases for
phenotypic traits
A gene is a sequence of DNA that directs the synthesis of a specific protein
-DNA is transcribed into RNA
-RNA is translated into protein
the presence and action of proteins determine the phenotype of an organism
Genetic information written in codons is translated into
amino acid sequences
The sequence of nucleotides in DNA provides a code for constructing a protein
-each amino acid is specified by a coon
-64 codons are possible
Some amino acids have more than one possible codon
Characteristics of the genetic code
-triplet: three nucleotides specify one amino acid
-61 codons correspond to amino acids
AUG codes for methionine and signals the start of transcription
- 3 "stop" codons signal the end of translation
Transcription produces genetic messages in the form of
RNA
Transcription
-the two DNA strands separate
-one strand is a pattern for producing RNA
-for A in DNA, U is replaced in RNA
RNA Polymerase
catalyzes in the reaction
Stages of transcription
-initiation:RNA polymerase binds to a promoter, where the helix unwinds and transcription starts
-Elongation:RNA nucleotides are added to the chain
-Termination:RNA polymerase reaches a terminator sequence and detaches from the template
Eukaryotic messenger RNA (mRNA) undergoes processing before leaving the nucleus
RNA splicing:removal of introns and joining of exons to produce a continuous coding sequence
Transfer RNA (tRNA) molecules serve as interpreters during
translation
Transfer RNA (tRNA) molecules serve as interpreters during translation
-transfer RNA (tRNA) molecules match an amino acid to its corresponding mRNA codon
Ribosomes build
polypeptides
Ribosomes carry out translation
-ribosomes have two subunits;small and large
-each subunit is composed of ribosomal RNAs and proteins
-ribosomes have binding sites for mRNA and tRNAs
Elongation adds amino acids to the polypeptide chain until a stop codon terminates
translation
Elongation adds amino acids to the polypeptide chain until a stop codon terminates translation
-elongation is the addition of amino acids tot he polypeptide chain
-elongation continues until the ribosome reaches a stop codon
-Termination
-the completed polypeptide is released
-The ribosomal subunits separate
_mRNA is released and can be translated again
Mutations can change the meaning of genes ( answer on 3)
a mutation is a change in the nucleotide sequence of DNA
-Base substitution: replacement of
one nucleotide with another
-effect depends on whether there is an amino acid change that alters the function of the protein 1 of 3
-deletions or intertions
-alter the reading frame of the mRNA, so that nucleotides are grouped in to different codons
-lead to significant chages in amino acid sequence downstream of mutation
-cause a nonfunctional polypeptide to be produced 2 of 3
Mutations can be
-spontaneous: due to errors in DNA replication or recombination
-induced by mutagens
High energy radiation
Chemicals 3 of 3
Nucleic acids are strands of repeated units/monomers. What are the monomers?
unit of DNA and RNA nucleotides
A strand of nucleotides has a _________backbone and _______that faces in one direction.
-----------
-----------
The DNA genotype is expredded as proteins, which provide the molecular bases for
phenotypic traits
A gene is a sequence of DNA that directs the synthesis of a specific protein
-DNA is transcribed into RNA
-RNA is translated into protein
the presence and action of proteins determine the phenotype of an organism
Genetic information written in codons is translated into
amino acid sequences
The sequence of nucleotides in DNA provides a code for constructing a protein
-each amino acid is specified by a coon
-64 codons are possible
Some amino acids have more than one possible codon
Characteristics of the genetic code
-triplet: three nucleotides specify one amino acid
-61 codons correspond to amino acids
AUG codes for methionine and signals the start of transcription
- 3 "stop" codons signal the end of translation
Transcription produces genetic messages in the form of
RNA
Transcription
-the two DNA strands separate
-one strand is a pattern for producing RNA
-for A in DNA, U is replaced in RNA
RNA Polymerase
catalyzes in the reaction
Stages of transcription
-initiation:RNA polymerase binds to a promoter, where the helix unwinds and transcription starts
-Elongation:RNA nucleotides are added to the chain
-Termination:RNA polymerase reaches a terminator sequence and detaches from the template
Eukaryotic messenger RNA (mRNA) undergoes processing before leaving the nucleus
RNA splicing:removal of introns and joining of exons to produce a continuous coding sequence
Homologous chromosomes bear the alleles for each
charater
For each pair of homologous chromosomes, alleles of a gene reside at the same locus
-homozygous individuals have the same allele on both homologues
-heterozygous individuals have a different allele on each homologue
The environment affects many characters
Phenotypic variations are influenced by the environment
-skin color is affected by exposure to sunlight
-susceptibility to diseases, such as cancer, has hereditary and environmental components
Gregor Mendel
discovered principles of genetics in experiments with the garden pea
Mendel showed that
parents pass heritable factors to offspring
Advantages of using pea plants
controlled matings
self fertilization or cross fertilization
observable characteristics with two distinct forms ( dominant and recessive phenotypes)
True breeding strains ( homozygous for the character being observed)
Mendel's law of segregation describes the inheritance of a
single character
Example of a monohybrid cross
Parental generation: purple flower x white flower
-F1 generation: all plants with purple flower
-F2 generation: 3/4 purple 1/4 white flowers