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Biology

Meiosis, mendel

QuestionAnswer
one of two or more possible forms of a character: a recognizable feature or characteristic of an organism Trait
the science of heredity and of the mechanisms by which traits are passed from parents to offspring genetics
type of organism whose ancestors are genetically uniform purebred
mating of two organisms cross
Mendel's first laws, stating that (1) organisms inherit two copies of genes, one from each parent, and (2) organisms donate only copy of each gene in their gametes because the genes separate during gamete formation law of segregation
the most basic physical unit of heredity: a segment of nucleic acids that codes for a functions unit of RNA and/or a protein gene
one of the alternative forms of a gene that governs a characteristic, such as hair color allele
describes an individual that has identical alleles for a trait on both homologous chromosomes homozygous
describes an individual that carries two different alleles of a gene heterozygous
the complete genetic material contained in an individual or species genome
the entire genetic makeup of an organism: also the combination of genes for one or more specific traits genotype
an organisms appearance or other detectable characteristic that results from the organism's genotype and the environment phenotype
in genetics, describes an allele that is fully expressed whenever the allele is present in an individual dominant
in genetics, describes an allele that is expressed only when no dominant allele is present in an individual recessive
a graphic used to predict the results of a genetic cross punnet square
a cross between individuals that involves one pair of contrasting traits monohybrid cross
cross between an organism with an unknown genotype and an organism with a recessive phenotype testcross
a cross between individuals that have different alleles for the same gene dihybrid cross
the law that states that genes separate independently of one another in meiosis law of independent assortment
the likelihood that a possible future event will occur in any given instance of the event: the mathematical ratio of the number of times one outcome of any event is likely to occur to the number of possible outcomes of the event probability
male gametes sperm
female gametes egg
one allele is not completely dominant over another. the heterozygous phenotype is somewhere in between the two homozygous phenotypes incomplete dominance
both alleles contribute to the phenotype of the organism codominance
can be used to predict the outcomes of genetic crosses, expressed as a fraction, ratio, decimal, or percentage: involves many trials principle of probability
production of gametes(sex cells-sperm and eggs) occurs in ovaries and testes meiosis
one form of a gene is usually dominant over the recessive form of the gene. Mendel discovered this when making his F1 generation from 2 purebred parents Principle of dominance
proves the genes segregate when gametes are formed. recessive alleles did not dissapear but reappeared in the F2 generation [at some point the T allele separated from the t allele Principle of segregation
Genes for differetn traits segregate independently from each other during the formation of gametes Principle of Independent assortment
cell that contains two sets of chromosomes, 2N is the number of chromosomes for a species diploid
threadlike structure inside the nucleus chromosomes
cell that contains one set of chromosomes, N is the number of chromosomes for a species haploid
means "four" tetrad
pairing of homologous chromosomes during meiosis synapsis
the exchange of genes by homologous chromosomes during meiosis crossing-over
homologous chromosomes seperate anaphase 1
chromosomes (not tetrads) line up at equator metaphase 2
crossing over begins and also synapsis occurs prophase 1
both daughter cells divide, forming four haploid cells telophase 2
centromeres divide and sister chromatids separate anaphase 2
spindle fibers move chromosomes to equator metaphase 1 and metaphase 2
tetrads line up at equator metaphase 1
daughter cells form, but chromosomes are in replication form telophase 1
cell that makes up all of the body tissues and organs, except gametes somatic cell
a haploid reproductive cell that unites with another haploid reproductive cell to form a zygote gamete
a mutation in which one nucleotide is substituted for another, can often be caught and fixed by dna polymerase point mutation
involves deletion or insertion of a nucleotide in the dna sequence and affects the polypoptide more and shifts. frameshift mutation
what type of cell is produced during meiosis? gametes and 4 haploid cells
will mutations in gametes be passed on to the offspring? it can be passed on to offspring in offspring or egg cells
will mutations in body cells be passed on to offspring? No they are not passed on to offspring
why is crossing over important? it guarantees the genetic variability and making us different
how does meiosis increase genetic variability? it increase genetic variability by crossing over and independent assortment
Created by: K0503295
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