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22 Cards in this Set
- Front
- Back
a segment of the chromosome turned around 180 within a chromsome
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Inversion
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requires a break at 2 points in the chromosome and then a reinsertion of the segment
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inversion
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true or false, heterozygotes that have inversion may produce abnormal offspring, will this have an affect on the offspring?
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Yes
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centromere is not part of the rearranged chrom. segment
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Paracentric inversion
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results in dicentric and acentric production of chromatids
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paracentric inversion
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What happens to the dicentric chromatid during anaphase?
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chromatids move in either direction
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what happens to the acentric chromatid during anaphase?
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it is lost or moves randomly to one pole or the other during anaphase.
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when centromere is part of the inverted segment
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paricentric inversion
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movement of a chromosome segment to a new location
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translocation
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an exchange that occurs between two non-homologous chromosomes. Genetic information is not lost or gained, but there is a rearrangement of genetic material.
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Reciprocal translocations
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occur when a chromosome breaks in one or more places and a portion is lost
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deletion
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during deletion, the segment of the chromosome that still has a centromere, will is be maintained or lost?
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maintained
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deletions that occur in the interior of the chromosome
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intercalary
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deletions that occur at the ends of chromosomes
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terminal
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occur when any part of a chrom. is present more than once in a genome
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duplication
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when are compensation loops formed?
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in deletions and duplications
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what do compensation loops do?
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they match homologous chroms. for synapsis
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True or false? Duplications occur because of unequal crossing over or through a replication error prior to meiosis?
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True
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Gene Family
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groups of continuous genes who products perform the same functino
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true or false, duplications can produce gene families?
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true
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occurs when breaks happen at the ends of the short arms of two non-homologous chromosomes. The small segments are lost and the larger segments fuse together at the centromeric region
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robertsonian translocation
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a translocation between chromosome 9 and 22 that is associated with myelogenous leukemia
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Phyladelhia chromosome
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