Set: kasby bo final ch 10

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All 46 terms

TermDefinition
punnett squarediagram showing the probabilites of the possible outcomes of a genetic cross
P generationparents of a genetic cross; the first two crossed
F1 generationfirst filial generation; offspring of the P generation
F2 generationseconf filial generation, offspring of the F1 generation
incomplete dominance(intermediate inheritance)neither allele is dominant; heterozygote shows intermediate phenotype; there is the possibility of having a third phenotype (blending). Ex: Red x White=Pink
homozygoushaving identical alleles for a gene
heterozygoushaving different alleles for a gene
purebredwhen the parents and grandparents are of the same breed
hybridoffspring of two different true-breeding varieties
dominantdescriptive of the allele in a heterozygous individual that appears to be the only one affecting a trait
recessivedescripitve of an allele in a heterozygous individual that does not appear to affect a trait
allelealternative form of a gene
genea DNA sequence that codes for a protein (polypeptide); mendel called them factors
hereditythe passing of traits to offspring
geneticsthe study of heredity
phenotypeobservable traits of an organism
genotypegenetic makeup of an organism; an organisms combination of alleles
Mendel's Laws of HeredityLaw of Indepentdent Assortment and Law of Segregation
Law of independent assortmenteach allele for a trait segregates into gametes independently of any other alleles, and allele for one trait does not necessarily end up in the same gamete as an allele for a different trait
law of segregationallele pairs (the two alleles for a heritable character) separate during Gametogenesis and end up in different gametes. A sperm or egg carries only one allele of each pair; this law states that allele pairs randomly form pairs at segregation
test cross (back cross)the mating of an individual of unknown genotype but dominant phenotype with a homozygous recessive individual. this cross is used when the genotype is not able to be determined by the information given
codominance inheritance patternboth alleles are dominant, and both phenotypes are present (not blended) Ex: roaning in horses ad cattle
incomplete dominance inheritance patternneither allele is dominant, heterozygote shows intermediate phenotype (Ex: blending) the F1 hybrids have an intermediate phenotype. the parent phenotypes appear in the F2 generation
structure of DNA moleculeDNA structure has sugars and phosphates that form the "backbone". nitrogenous bases are down the center- four different types:adenine, thymine, guanine, and cytosine. DNA molecule consists of a double helix which is an intertwined backbone that forms a helix
discovered double helixwatson and crick
DNA different from RNADNA has deoxyribose sugar, RNA has ribose sugar. DNA has thymine, RNA has uracil; DNA is double stranded, RNA is single stranded
function of tRNA(transfer RNA)"interpreter"; translates nucleic acid language into amino acid language; brings amino acids from cytoplasm to ribosome/mRNA complex; there are 3 tRNA that match an mRNA codon. tRNA tells mRNA which amino acid to pick up from the cytoplasm. Special enzymes "charge" the tRNA; there is one amino acid per tRNA
purpose of mRNAit's complementary to coding strand; the base pairing rules are followed= uracil replaces thymine; when mRNA transcript is formed, it falls off DNA strand when completed
DNA replicationprocess by which DNA makes and exact copy of itself; procces occurs during the S phase of Interphase; cell does for growth, repair, and reproduction
end result of replicationtwo new DNA strand form; strands are complementary copies of parent strands; one strand of parent DNA combines with one strand of new DNA; this is semiconservative replication
transcriptionprocess by which DNA makes a single RNA molecule(different form, same message); Only one DNA strand is copied-that strand is a coding or template strand. mRNA is complementary to coding strand. Thymine is replace with Uracil.DNA helix unwinds and exposes the bases; free nucleotides in the cytoplasm base-pair with DNA nucleotides on the coding strand. RNA polymerase creates a bond b/w the DNA and RNA bases. When mRNA transcript is formed, it falls off. DNA rezips to the original double helix. end results in a single stranded RNA molecule.
translationduring, codond (set of three bases in mRNA that correspond to triplets in DNA) are decoded into amino acids to make proteins.
codonset of three bases in mRNA that correspond to triplets in DNA
anticodonin tRNA, a triplet of nitrogenous bases that is complementary to a specific codon in mRNA
nucleotidebuilding block (monomer) of nucleic acid polymers
genea DNA sequence that codes for a protein(polypeptide)
adeninematches with thymine
guaninematches with cytosine
in RNA, thymine base isreplaced with uracil
proteins(polypeptides)genes code for these
mutationschanges in the DNA sequence of a gene; may be harmful, helpful, silent; two general types: base substitution (not usually harmful) and base insertion or deletion
base substitutions mutationone base (or nucleotide) is replaced by another; changes amino acid, may or may not change the protein; can be silent, minor, or drastic effect.
base insertions or deletions mutationadding or removing one or more bases alters the triplet in DNA and codon reading frame in the mRNA(frameshift mutation); this affects amino acid sequence, there are new amino acids made. this mutation "regroups" bases into different codons. no amino acids(nonsense codon) the protein is not completed or non-working
cancercaused by carcinogens(the mutations that cause this); malignant and benign tumors
malignant tumortumors that can harm the body
benign tumorstumors that are present in or on the body but have no harmful effects.
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Set Information

Terms 46
Creator lauren_lopez
Created June 2, 2009
Groups None
Subject bio final ch 10 and 11
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Most Missed Words

  1. anticodon in tRNA, a triplet of nitrogenous bases that is complementary to a specific codon in mRNA - 1 miss
  2. Law of independent assortment each allele for a trait segregates into gametes independently of any other alleles, and allele for one trait does not necessarily end up in the same gamete as an allele for a different trait - 1 miss
  3. gene a DNA sequence that codes for a protein (polypeptide); mendel called them factors - 1 miss
  4. base substitutions mutation one base (or nucleotide) is replaced by another; changes amino acid, may or may not change the protein; can be silent, minor, or drastic effect. - 1 miss