Across |
1. | visible, observable trait of an organism that masks a recessive form of the trait |
5. | hidden trait of an organism that is masked by a dominant trait |
7. | passing on of characteristics from parents to offspring |
8. | random error or change in the DNA sequence that may affect whole chromosomes or just one gene |
9. | in DNA, the two twisted, ladder-shaped nucleotide strands held together by hydrogen bonds between the bases |
11. | process in which the two strands of the double helix separate and bases pair with free nucleotides to form two molecules of DNA, each identical to the original molecule |
15. | graphic representation showing patterns of inheritance in a family or breeding group |
16. | equal expression of both alleles |
19. | absence of a chromosome |
20. | presence of more than two alleles for a given genetic trait in a species |
21. | the RNA that composes ribosomes |
22. | delivers amino acids to the ribosome for protein synthesis |
27. | major source of genetic variation resulting from crossing over or random assortment |
29. | structures having a common evolutionary origin |
32. | Mendelian principle explaining the disappearance of a specific trait in the F1 generation and its reappearance in the F2 generation |
35. | error in the DNA sequence that affects only a single base pair |
36. | cell division in which one diploid (2n) cell produces four haploid (n) cells called sex cells |
39. | reproductive pattern in which haploid gametes fuse to produce a diploid zygote, which then develops by mitosis into a new organism |
40. | process in which the order of bases in mRNA codes for the order of amino acids in protein |
42. | a cell of an organism that has half the number of chromosomes (n) |
43. | male sex cell |
45. | mating between closely related individuals to produce pure lines |
47. | fertilization between two organisms to study the inheritance of two different traits |
48. | offspring produced when two varieties of plants or animals, or closely related species, are mated |
50. | mutation affecting gene distribution to gametes during meiosis, most commonly by deletions, insertions, inversions, or translocations |
51. | determination of a given trait, such as skin color or height, produced by the interaction of many genes |
52. | carries protein synthesis information from DNA to the ribosomes |
53. | fusion of male and female gametes |
54. | exchange of genetic material by non-sister chromatids during late prophase I of meiosis, resulting in new combinations of alleles |