ch 14 Flashcards
what affect can chromosomal rearrangement?
change the structure of the chromosome and can either cause a loss or gain of part of the chromosome that is caused by chromosomal breakage or illegitimate -> can lead to mutations
what are illegitmate CO?
regions of repeats on the same chromosome or a separate one that can cause un=/illgitamete CO
Chromosomal deletion
Part of the chromosome is missing due to breakage and the parts that are leftover are glued back together.
can hemizygotes survive chromosome deletion? why do mutant phenotypes happen
no
Mutant phenotypes can happen because of haploinsufficiency (gene dosage is too low), vulnerability to mutation (only 1 normal if something happens to it then oh well), and loss of dominant allele (recessive may show since the dominant allele was deleted)
what is chromosomal inversion?
The sequences are facing in opposite directions where the breakage flips around and reattaches.
what are the two types of chromosomal inversion?
peri(includes centromere)/paracentric (excludes centromere)
what kind of affect does chromosomal inversions have on the phenotype?
if it is a large enough region it can result in lethality but this only really happens when the inversion is in the middle
what are the two types of paracentric fragments?
acentri: (lacks centromere) is lost in the gamete
-dicentric (lacks 2 centromeres and happens during anaphase) - breakage at random points
chromosomal duplications
the repeats on homologous chromosomes happen in multiple places causing uneven CO
what are the weo types of chromosomal duplications?
-tandem duplication :duplicated regions are next to one another and are on the same chromosome -> this can lead to unequal CO)
-non tandem repeats (duplicated regions that do not lie next to each other on other chromosomes)
what kind of effect can chromosomal duplications have on the phenotype?
- does not usually affect the progeny but it can when the trait is senstitive to the increased numbers or if the gene is on the border border of the duplication and has alternative expression because of the new chromosome environment.
chromosomal translocation
-The two chromosomes are not homologous at all but have similar repeats
-Two nonhomologous chromosomes interact and so part of one chromosome is transferred to another or both chromosomes swap material
Pseudolinkage
genes on either side of the breakpoint behave as if they are linked (genes that are on separate chromosomes act like they are linked)
Transposable elements
small DNA segments capable of relocating within the genome, either on the same chromosome or a different one, akin to their dynamic movement. Their mobility frequently disrupts normal gene expression patterns.
what are the two ways transposable elements can move around?
-Retrotransposons: transpose by reverse transcription of RNA intermediate
-DNA transposons:move their DNA directly without the requirement of an RNA intermediate