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biology
chapter 10
| Question | Answer |
|---|---|
| one of the possible forms of a gene-determines a trait- genes can have diff. numbers of them | allele |
| process by which reproductive cells are formed | meiosis |
| graduate student at colombia university- 1902- identified that genes were located on chromosomes | walter sutton |
| what is the chromosome theory of heredity | genes are located on chromosomes-a gene may exist in several forms or alleles- each chromosomes contains just one of the alleles for each of its genes |
| american geneticist and his associate, alfred sturtevant studied the tiny fruitfly. | thomas huntmorgan |
| what are the 3 reasons to study fruitflys | -easy to breed-produce every 4 weeks, 300 offspring- chromosome easy to study, largest chromosome found in animal cells. |
| individuals with new cominations of genes | recombinants |
| an exchange of alleles happens during 1st meiotic division when homologous chromosomes are paired-produces new combinations of alleles on each chromosome and increases genetic variety | crossing over |
| 1905, american biologist-discovered sex chromosomes-noticed cells of female mealword had 20 large chromosomes | Nettie Stevens |
| a change in the genetic material of a cell-may be harmful | mutations |
| mutations that affect the reproductive or germ cells | germ mutations |
| mutations that affect the other cells of the body, not inheritable-many cancers caused by this | somatic mutations |
| what 2 levels do mutations occur on? | 1-involve segments of chromosomes, whole chromosomes and entire sets - 2-involve individual genes |
| what are the 4 types of chromosomal mutation? | deletion, duplication, inversion, translocation |
| loss of part of a chromosome | deletion |
| a segment of chromosome is repeated | duplication |
| part of a chromosome becomes oriented in the reverse of its usual direction | inversion |
| part of one chromosome breaks off and attaches to another nonhomologous chromosome | translocation |
| the failure of homolougus chromosome to separate normally during meiosis | nondisjunction |
| condition in which an organism has extra sets of chromosomes- almost always fatal in animals | polyploidy |
| a change involving the nuceotides of dna | gene mutation |
| a gene mutation that affects single nucleotide | point mutation |
| a gene mutation involving an addition or deletion that alters every codon from the point of mutation on; an change the polypeptide product produced by the gene | frameshift mutation |
| what 5 things can cause mutations | radiation, viruses,hight temp, certain chemicals, environmental pollunts |
| any substance or condition that disrupts the normal formation of dna. | mutagen |
| an oranism that has a mutation | mutant |
| inheritance in which an active allele does not entirely compensate for an inactive allele | incomplete dominance |
| written as capitak allele with subscripts or superscripts | codominate alleles |
| traits that are control by 2 or more genes (ex. the shape of your nose) | polygenic inheritance |
| nobel prize 1983-jumping genes (genes move) | barbara mcclintock |