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Hon. Bio. Vocab.

Chapters 13-15. by Kelsey Q. W.

QuestionAnswer
Gene discrete unit of hereditary information consisting of a specific nucleotide sequence in DNA
Gene Locus gene’s specific location along the length of a chromosome
asexual reproduction a single individual is the sole parent and passes copies of all its genes to it’s offspring
clone a group of genetically identical individuals
sexual reproduction Two parents give rise to offspring that have unique combinations of genes inherited from the two parents
Life Cycle the generation-to-generation sequence of stages in the reproductive history of an organism, from conception to production of it’s own offspring
karyotype ordered displays of an individual’s chromosomes
homologous chromosome chromosome pairs of the same length, centromere position, and staining pattern that possess genes for the same characters at corresponding loci. One homologous chromosome is inherited from the organism’s father, the other from the mother
amniocentesis A technique for determining genetic abnormalities in a fetus by the presence of certain chemicals or defective fetal cells in the amniotic fluid, obtained by aspiration from a needle inserted into the uterus
sex chromosome One of the pair of chromosomes responsible for determining the sex of an individual
autosome A chromosome that is not directly involved in determining sex, as opposed to a sex chromosome
fertilization The union of haploid gametes to produce gametes to produce a diploid zygote
haploid Cell containing only one set of chromosomes
diploid A cell containing two sets of chromosomes.
meiosis Two stage type of cell division in sexually reproducing organisms that results in cells with half the chromosome number of the original cell
alternation of generations Life cycle in which there is both a multicellular diploid form, the sporophyte, and a multicellular haploid form, the gametophyte; characteristic of plants.
sporophyte The multicellular diploid form in organisms undergoing alternation of generations that results from a union of gametes and that meiotically produces haploid spores that grow into the gametophyte generation
gametophyte The multicelular haploid form in organisms undergoing alternation of generations that mitotically produces haploid gametes that unite and grow into the sporophyte generation
crossing over The reciprocal exchange of genetic material between nonsister chromatids during synapsis of meiosis I.
synapsis The pairing of replicated homologous chromosomes during prophase I of meiosis
tetrad A paired set of homologous chromosomes, each composed of two sister chromatids. Tetrads form during prophase of meiosis
cell division The reproduction of cells
character A heritable feature
true-breeding Plants that produce offspring of the same variety when they self-pollinate
hybrid The offspring of two different types of parents
allele Alternate versions of a gene
dominant A gene that is always going to take precedence against any other gene.
Recessive A gene that will not take precedence unless there is only the recessive type.
Law of Segregation Mendel's first law, stating that allele pairs separate during gamete formation, and then randomly re-form pairs during the fusion of gametes at fertilization.
Homozygous Having two identical alleles for a given trait
Heterozygous having two different alleles for a genetic character
Phenotype The physical and psychological traits of an organism
Genotype The genetic makeup of an organism
Dihybrid Cross A breeding experiment in which parental varieties differing in two traits are mated.
Probability The odds of a certain outcome of an event.
incomplete Dominance A type of inheritance in which F1 hybrids have an appearance that is intermediate between the phenotypes of the parental varieties.
Pleiotropy The ability of a single gene to have multiple effects
Polygenic Inheritance An additive effect of two or more gene loci on a single phenotypic character.
Pedigree A family tree describing the occurrence of heritable characters in parents and offspring across as many generations as possible.
Carrier An organism that has the genes for a trait but is not active in the organism
Chromosome Theory of Inheritance Mendolian Genes have specific loci on chromosomes
Wild Type An individual with the normal phenotype
Sex-linked gene A gene located on a sex chromosome
recombinant An offspring whose phenotype differs from that of the parents
Independent Assortment All the possible assortments of maternal and paternal chromosomes
Genetic Map an ordered list of the genetic loci along a particular chromosome
Nondisjunction An accident of meiosis or mitosis, in which both members of a pair of homologous chromosomes or both sister chromatids fail to move apart properly.
Trisomic A chromosomal condition in which a particular cell has an extra copy of one chromosome, instead of the normal two; the cell is said to be trisomic for that chromosome.
Aneuploidy A chromosomal aberration in which certain chromosomes are present in extra copies or are deficient in number.
Polyploidy A chromosomal alteration in which the organism possesses more than two complete chromosome sets.
Down Syndrome A human genetic disease resulting from having an extra chromosome 21, characterized by mental retardation and heart and respiratory defects.
Turner Syndrome A syndrome that results from monosomy X. Only visible monosomy in humans
Keinfelter Syndrome When there is an extra X chromosome in a male
Genomic Imprinting The parental effect on gene expression. Identical alleles may have different effects on offspring, depending on whether they arrive in the zygote via the ovum or via the sperm.
Extra-Nuclear Genome Gene found on small circles of DNA in mitochondria and in plants plastids
Created by: villanova
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