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55 Cards in this Set

  • Front
  • Back
Cell Division
When a cell undergoes reproduction.(2) the reproduction of a cell through duplication of the genome and division of the cytoplasm.
Chromosomes
The structures that contain most of the cells DNA.(2) A threadlike, gene-carrying structure found in the nucleus of a eukaryotic cell and most visible during mitosis and meiosis;also, the main gene-carrying structure of a prokaryotic cell. A chromosome consists of one wery long piece of chromatin, a combination of DNA and protien.
Asexual Reproduction
The creation of genetically identical offspring by a single parent.
Sexual Reproduction
Requires fertilization of an egg by a sperm.
Chromatin
Fibers composed of roughly equal amounts of DNA and protein molecules.
Sister Chromatids
One of the two identical parts of a duplicated chromosome in a eukaryotic cell.Prior to mitosis, sister chromatids remain attached to each another at the centromere.
Centromere
The region of a duplicated chromosome where two sister chromatids are joined.
Cell Cycle
An ordered sequence of events that extends from the time a cell is first formed from a dividing parent cell until it's own division into two cells.
Interphase
This is a time when a cell's metabolic activity is very high and the cell performs it's various functions within the organism.
Miotic Phase
The part of the cell cycle when the cell actually divides.
Mitosis
The nucleus and it's contents divide and are evenly distributed forming two daughter nuclei.
Cytokinesis
The cytoplasm is divided into two.
Interphase
The period of cell growth, when the cell synthesizes new molecules and organelles.
Prophase
Changes occur in both the nucleus and the cytoplasm
Prometphase
The nuclear envelope breaks into fragments and disappears
Metaphase
The miotic spindle is fully formed
Anaphase
When the two centromeres of each chromosome come apart.
Telophase
The cell elongation that started in the Anaphase continues
Miotic Spindle
A football shaped structure of microtubules that guides the separation of the two sets of daughter chromosomes.
Centrosomes
(1)Clouds of cytoplasmic material that in animal cells contain pairs of centrioles. (2) Material in the cytoplasm of a eukaryotic cell that gives rise to microtubules; important in mitosis and meiosis; also called the microtubule-organising center.
Cell Cycle Control System
A cyclically operation set of molecules in the cell that both triggers and coordinates key events in the cell cycle.
Tumor
An abnormally growing mass of body cells.
Benign Tumor
Abnormal cells that remain at the original site.
Malignant Tumor
An abnormal tissue mass that can spread into neighboring tissue and to other parts of the body.
Metastasis
The spread of cancer cells beyond their original site.
Carcinomas
Cancers that originate in the originate in the external or internal coverings of the body.
Sarcomas
Arise in tissues that support the body
Leukemias and Lymphomas
Cancers of blood-forming tissues, such as bone marrow, spleen, and lymph nodes.
Somatic Cell
A typical body cell that has 46 chromosomes.
Homologous Chromosomes
The two chromosomes that make up a matched pair in a diploid cell.
Locus
The particular site where a gene is found on a chromosome.
Sex Chromosomes
What determines an individuals sex.
Autosomes
The 22 remaining chromosomes foind in both males and females.
Life Cycle
The sequence of stages leading from the adults of one generation to the adults of the next.
Diploid
A cell containing two homologous sets of chromosomes.(2) In an organism that reproduces sexually, a cell containing two homologous sets of chromosomes, one set inherited from each parent; a 2n cell.
Gametes
Egg and sperm cells.
Haploid
A cell with a single chromosome set.(2) In the life cycle of an organism that reproduces sexually, a cell containing a single set of chromosomes; a n cell.
Fertilization
When a haploid cell from the father fuses with a haploid cell from the mother.
Zygote
A fertilized egg.
Alleles
The alternative versions of a gene
Meiosis
A type of cell division that produces haploid gametes in diploid organisms.
Crossing over
An exchange of corresponding segmentsbetween nonsister chromatids of homologous chromosomes,
Chiasma
The microscopially visible site where crossing over has occured between chromatids of homologous chromosomes during prophase I of meiosis.
Tetrad
A paired set of homologous chromosomes, each composed of two sister chromatids. Tetradsform during prophase I of meiosis,when crossing over may occur.
Genetic recombination
The production, by crossing over and/or independent assortment of chromosomes during meiosis, of offspring with allele combinations different from those in the parents. The term also may be used more specifically to mean the production by crossing over of eukaryotic or prokaryotic chromosomes with gene combinations different from those in the original chromosomes.
Karotype
A display of micrographs of the metaphase chrosomes of a cell, arranged by size and centromere position. Karotypes may be used to identify certain chromosomal abnormalities.
Trisomy 21
See Down syndrome
Down Syndrome
A human genetic disorder resulting from the presence of an extra chromosome 21; characterized by heart and respiratory defects and varying degrees of mental retardation.
Nondisjunction
An accident of meiosis or mitosis in which a pair of homologous chromosomes or a pair of sister chromatids fail to seperate at anaphase.
Polypoid
Am organism that has more than two complete sets of chromosomes as a result of an accident of cell division.
Deletion
The loss of one or more nucleotides from a gene by mutation; the loss of a fragment of a chromosome.
Duplication
Repetition of part of a chromosome resulting from fusion with a fragment from homologous chromosome; can result from an error in meiosis or from mutagenesis.
Inversion
A change in a chromosome resulting from reattachment of a chromosome fragment to the original chromosome, but in a reverse direction. Mutagens and errors during meiosis can cause inversions.
Translocation
(1) During protien synthesis,the movement of a tRNA molecule carrying a growing polypeptide chain from the A site to the P site on a ribosome.(The mRNA travels with it.) (2) A change in a chromosonoe resulting from a chromosomal fragment attaching to a nonhomologous chromosome; can occur as a result of an error in meiosis or from mutagenesis
Mutagen
A chemical or physical agent that interacts with DNA and causes a mutation.