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Biology 15

QuestionAnswer
genetics scientific study of heredity and variation
heredity the transmission of traits from one generation to the next
variation demonstrated by the differences in appearance that offspring show from paresnts and sibilings
in literal sense children do no inherit particular physical traits from their parents but inherit genes
genes the units of heredity and are made up of segments of DNA
genesrs are passed to next generation via reproductive cells called gametes
locus specific location on a certain chromosome, each gene has
asexual reproduction single individual passes genes to its offspring without fusion of gametes
clone group of genetically identical individuals from same parent
sexual reproduction 2 parents give rise to offspring that have unique combinations of genes inherited from 2 parents
life cycle generation to generation sequence of stages in the reproduction history of an organism
humans somatic cells have 23 pairs of chromosomes
karytotype an ordered display of the pairs of chromsomes from a cell
homologous chromosomes (homologs) 2 chromosomes in each pair
chromosomes in a homologous pair are the same length and shape and carry genes controlling the same inherited characters
sex chromosomes determine sex of the idvidiual and are called X and Y
females have a homologous pair of X chromosomes
males have one X and one Y chromosome
autosomes the remaining 22 pairs of chromosomes
each pair of homologous chromsomes includes one chromosome from each parent
number of chromosomes 46 chromomes in a human somatic cells- two sets of 23, one from mom and one from dad
diploid cells (2n) has two sets of chromosomes
for humans, diploid number is 46 (2n=46)
when dna synthesis has occurred in a cell each chromosomes is replicated and consists of 2 indentical sister chromatids
haploid (n) a gamete which contains a single set of chromosomes
humans haploid number 23 n=23
eat set of 23 consists of 22 auntosomes and a single sex chromsome
ovum unferitilized egg with the sex chromosome of X
a sperm cell sex chromosome is X or Y
fertilization the union of gametes (sperm and egg)
zygote fertilized egg which has one set of chromosomes from each parent
zygote produces somatic cells by mitosis and develops into an adult
at sexual maturity the ovaries and testes produce haploid gametes
gametes are the only types of cells produced by meiosis
meiosis results in one set of chromsomes in each gamete
fertilization and meiosis altnerate in sexual life cycles to maintain chromosome number which is common to all organisms that reproduce sexually
the 2 main types of sexual life cycles differ in timing of meiosis and fertilization
gametes are the only haploid cells in anmials and produce by meiosis and undergo no further celldivision before fertilization
gametes fuse to form a diploid zygote that dividies by mitosis and develop into a multicellular organsims
alnternation of generations exhibited by plants and some algae and is a life cycle including both a diploid and haploid multicellular stage
sporophyte a diploid organism which makes haploid spores by meiosis
gametophyte a haploid orgnaims which each spore grows in to by mitosis
a gametophyte makes haploid gametes by mitosis
fertilization of gametes in a plant result in a diploid sporophyte
in most fungi and some protist the only diploid stage is the single celled zygot, there is no multicellular diploid stage
the zygote produces haploid cells by meiosis
haploid cells grow by mitosis into a haploid multicellular organism and produces gametes by mitosis
depending on the type of life cycle either haploid or diploid cells can divide by mitosis but only diploid cells can undergo meiosis
in all three life cyccles halving and doubling of chromosomes contributes to genetic variation in offspring
like mitosis, meiosis is preceded by the replication of chromosomes
meiosis takes place in 2 sets of cell divisions, meiosis I and meiosis II
the two cell divisions of meiosis result in 4 daughter cells rather than two daughter cells in mitosis and each daughter cell has only half as many chromosomes as the parent
after chromosomes duplicate meisosi I and meiosis II follows
meiosis I reductional division, homologs pair up and separate resulting in two haploid daughter cells with replicated chromosomes
meiosis II equaitonal division, sister chromatids sepearate
result of meiosis I and II four haploid daughter cells with unreplicated chromosomes
meiosis I is preceded by interphase, when the chromosomes are duplicated to form sister chromatids
sister chromatids are genetically identical and joined at the centromere
centrosome replicated to form two centrosomes
division in meiosis I occurs in 4 phases, prophase I, metaphase I, anaphase I, and Telophase I & cytokinesis
Prophase I typically occupies mote that 90% of the time required for meiosis, chromosomes begin to condense, homologous chromosomes loosely pair up in synpasis aligned gene by gene
crossing over (Prophase I) nonsister chromatids exchange DNA segments
each pair of chromsomes forms a (Prophase I) tetrad (group of 4 chromosomes)
each tetrad (Prophase I) has one or more chiasmata (x shaped regions where crossing over occurred)
Metaphase I tetrads line up at metaphase plate with on chromosome facing each pole
microtubules (metaphase I) from one pole are attached to kinetochore of one chromosome of each tetrad and from the other pole are attached to the kinetochore of the other chromosome
anaphase I pairs of homologous chromosmes separate, one chromosome moves toward each pole guided by the spindle apparatus and siter chromatids remain attached at the centromere and move as one toward pole
telophase I each half of the cell has a haploid set of chromosomes, each with 2 sister chromatids
cytokinesis occurs simultaneously forming 2 haploid daughter cells
animal cells vs plant cells animal cells: cleavage furrow forms plant cells: cell plate forms
at the end of meiosis I and beginning of meiosis II no chromosomes replicate because the chromsomes are already replicated
division in meiosis II occurs in 4 phases, prophase II, metaphase II, anaphase II, telophase II and cytokinesis
prophase II spindle apparatus forms then chromsomes composed of 2 chromatids move toward the metaphase plate
metaphase II sister chromatids are arranged at the metaphase plate, the kinetochores of sister chromatids attach to microtubules extending from opposite poles
anaphase II the sister chromatids separate and move toward opposite poles as individual chromosomes
telophase II the chromsomes arrive at opposite poles and nuclei forms and chromosomes begin to descend
cytokinesis separates the cytoplasm
at the end of meiosis there are four daughter cells, each with a haploid set of unreplicated chromsomes and are genetically distinct from the others daughters and parent cells
mitosis conserves the number of chromosome setse producing cells that are genetically identical to the parent cell
meiosis reduced number of chromosomes sets from two (diploid) to one (haploid)producing cells that differ genetically from each other and from the parent cell
the 3 events that are unique to meiosis all occur in meiosis I
1st event that are unique to meiosis synapsis and crossing over in prophase I: homologougenetic infos chromsomse physically connect and exchange
2nd event that are unique to meiosis at the metaphase plate, there are paired homologous chromosomes( tetrads) instead of individiaul replicated chromosomes
3rd event that are unique to meiosis at anaphase I, it is homologous chromsomes instead of sister chromatids that separate
sister chromatid cohesion allows sister chromatids of a single chromosome to stay together through meiosis I
cohesins protein complexes which are responsible for cohesion of sister chromatids
in mitosis cohesins are cleaved at the end of metaphase
in meiosis cohesins are cleaved along the chromosome arm in anaphase I (separation of homologs) at the centromeres in anaphase II (separation of sister chromatids)
mutations changes in an organisms dna, the orginal source of genetic diversity
alleles different version of genes created by mutations
genetic variation produced by reshuffling of alleles during sexual reproduction
what is responsible for most of variations that arises in each generation behavior of chromsomes during meiosis and fretilization
3 mechanisms that contribute to genetic variation independent assortment of chromosomes , crossing over, and random fertilization
homolgous pairs of chromsomes orient randomly at metaphase I of meiosis
in independent assortment each pair of chromosomes sort material and paternal homologs into daughter cells independently of the other pairs
number of combinations possible when chromsomes assort independenlty into gametes is 2^n where n is the haploid number
for humans there are more than 8 million 2^23 possible combinations of chromosomes
recombinant chromsomes combination of dna inherited from each parent which is produced by crossing over
crossing over begins very early in prophase I as homologous chromsomes pair up gene by gene
during crossing over homologous portions of 2 nonsister chromatids trade places
crossing over contributes to genetic variation by combining DNA from 2 parents into a single chromosome
random fertilization adds to genetic variation because any sperm can fuse with any ovum (unfertilized egg)
fusion of 2 gametes each with 8.4 million possible chromosome combinations from independent assortment- produces a zygote with any of about 70 trillion diploid combinations
crossing over adds even more vatiation
each zygote has a unique genetic identity
natural selection results in the accumulation of genetic variations favored by the environment
sexual reproduction contributes to contributes to the genetic vaiation in a population which originates from mutations
Created by: newmee32
 

 



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