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41 Cards in this Set

  • Front
  • Back
DNA is a single strand copy of a gene found in the genetic materials and is translated into a protein
false- RNA
mRNA is a molecule that carries the genetic info from DNA and as used as a template for protein synthesis
true
Eukaryotic cells differ from prokaryotic cells in that only the former contain a nucleus
true
DNA duplication takes place in the M phase of the cell cycle
false- s phase
In a karyotype, the location of the breast cancer susceptibility gene (BRCA1) is given as 17q21. This means the gene is located on chromosome 21.
false chromosome 17
meiosis minimizes genetic variation among sexually reproducing populations
false- meiosis maximizes genetic variation
in a testcross, the unknown genotype is crossed with a homozygous recessive individual to determine genotype
true
pleiotropy happens when the phenotype can be influenced by many genes
false- epistasis.....pleiotropy is one gene affects many phenotypes
if recombination frequency is 30.5% the distance between these two genes is 30.5 cM
true
genes that are tightly linked recombine often
false- linked recombine occasionally
in eukaryotic cells, DNA is only found in the nucleus
false- mitochondria, chloroplasts
alternative forms of a gene are called a locus
false- allele
meiosis- 4 haploid
mitosis- 2 diploid
true
human genome has 24 pairs of chromosomes
false- 23 pairs
what is correct order from smallest level?:
chromosome, genes, genome, nucleotides
nuleotides
genes
chromosome
genome
what are dna base pairs?
rna base pairs?
A/T and C/G
A/U and C/G
a process that occurs in meiosis but not in mitosis?
pairing of homologous chroms
crossing over happens during which stage of cell division
prophase 1
for any given gene, the principle of segregation predicts that gametes produced as a result of meiosis will contain
a single allele of a gene pair
the interaction between non-allelic genes in their effects on a trait is called
epistasis
in a pop carrying a dominant mutant allele, only 70% of the people carrying the allele show the phenotype. this exhibits
incomplete penetrance
in dihybrid crosses, 9:3:3:1 indicates
independent assortment
a cross between two heterozygotes for one trait yields a phenotypic ratio of 2:1. whats the best explanation?
the dominant trait is lethal in homozygous form
in maize the genes A and B are so tightly linked that virtually no crossovers occur between them. a dihybrid Ab/aB is testcrossed to ab/ab. the percentage of progeny with A-B- genotype will be?
0%
when only males exhibit a recessive trait this is called
x linked recessive
maximum recombination frequency between two genes is
50%
compared to heterochromatin, euchromatin is ...
less densly stained and less densly packed
the failure of chromosomes to separate during meiosis is known as what?
non-disjunction
in a sweet pea experiment progeny revealed a ratio of roughly 23:1:1:7. this is an idication of what basic trait?
linkage
crossing over occurs in which stage of meiosis 1?
pachynema
what happens to chromosomes in each stage?
leptonema
zygonema
pachynema
diplonema
diakinesis
chroms are already duplicated
pairing is initiated
pairing and crossing over
held by centromere and
repulsion begins
chroms move to equitorial plane
recombinant chromosome
when two different chromosomes are next to each other and they trade genes "crossing over"
linkage
genes on same chromosome
coupling
homologous linkages (dominant or recessive)
repulsion
heterozygous linkage (dominant linked to a recessive)
crossing over is ______ likely to occur if genes are close together on a chrom
less
crossing over is ______ likely to occur if genes are far apart on a chrom
more
to test for recombination/crossing over, what is crossed with what?
heterozygous female with a homozygotus recessive male
if crossing over occurs progeny will be...
50% wild type
50% mutant cross overs
in drosophila, recombination is not seen in
the male flies
interface
the difference between the observed and expected crossovers.
1-(observ/expected)