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Genetics & Mendel
Ch 12 Inheritance/Meiosis
| Question | Answer |
|---|---|
| The scientific study of biological inheritance | Genetics |
| process of sexual reproduction in which male and female reproductive cells join to form a new cell | fertilization |
| specific characteristic of an individual | trait |
| offspring of crosses between parents with different traits | hybrid |
| sequence of DNA that codes for a protein and thus determines a trait; factor that is passed from parent to offspring | gene |
| one of a number of different forms of a gene | allele |
| Mendel’s second conclusion, which states that some alleles are dominant and others are recessive | principle of dominance |
| separation of alleles during gamete formation | segregation |
| sex cell with haploid number of chromosomes | gamete |
| exhibits the dominant trait Capital letter genotype | dominant allele |
| the trait that can be masked by the dominant trait known by lowercase letter | recessive allele |
| the likelihood that a particular event will occur | probability |
| having two identical alleles for a particular gene | homozygous |
| having two different alleles for a particular | heterozygous |
| physical characteristics of an organism | phenotype |
| genetic makeup of an organism | genotype |
| diagram that can be used to predict the genotype and phenotype combinations of a genetic cross | Punnett Square |
| one of Mendel’s principles that states that genes for different traits can segregate independently during the formation of gametes | Principle of Independent Assortment |
| situation in which one allele is not completely dominant over another allele | incomplete dominance, |
| situation in which the phenotypes produced by both alleles are completely expressed | Codominance |
| a gene that has more than two alleles | multiple alleles |
| trait controlled by two or more genes | polygenic traits |
| type of chromosomes in which one set comes from the male parent and one set comes from the female parent | homologous Sounds like "home-ah-lo-gus" |
| a cell that contains two sets of homologous chromosomes (2n) | diploid |
| a cell that contains only a single set of genes (n) | haploid |
| process in which the number of chromosomes per cell is cut in half through the separation of homologous chromosomes in a diploid cell | Meiosis |
| structure containing four chromatids that forms during meiosis or homologous pair of chromosomes | tetrad |
| process in which homologous chromosomes exchange portions of their chromatids during prophase I of meiosis or segments of non-sister chromatids break and reattach to the other chromatid | crossing-over |
| Genotype with 2 dominant alleles (Ex: TT) | Homozygous Dominant |
| Genotype with 1 dominant allele and one recessive allele (Ex: Tt) | Heterozygous |
| Genotype with 2 recessive alleles (Ex: tt) | Homozygous Recessive |
| maternal | mother |
| paternal | father |
| female gamete or female sex cell | egg cell (ovum) |
| location or position of a gene | locus |
| first 22 pairs of homologous chromosomes | autosomes |
| the 23rd (or last) pair of homologous chromosomes | sex chromosomes |
| male gamete | sperm cell |
| process of production and maturation of sperm | Spermatogenesis Sounds like "sperm-at-o-gen-uh-sis |
| Process of production and maturation of egg cell (or ovum) | Oogenesis Sounds like "o-o-gen-uh-sis" |
| Type of human body cell with the "normal" amount of chromosomes (2n) | Somatic cells |
| two chromatids joined by a common centromere | sister chromatids |
| chromatids of the other chromosome of a homologous pair | non-sister chromatids |
| location of crossing over or location where chromosomes touch each other and exchange genes | Chiasmata (chiasma) Sounds like "khi-as-mata" |
| female sex chromosome | XX |
| male sex chromosome | XY |
| egg cell and sperm cell fuse together to form a | zygote |
| the process of the egg cell (ovum) and sperm cell fusing | fertilization |