polyploidy …more than two haploid sets of chromosomes are present, –2n = diploid, –3n =...
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Polyploidy
…more than two haploid sets of chromosomes are present,
– 2n = diploid,– 3n = triploid, – 4n = tetraploid, – etc.
Autopolyploidy
...polyploidy resulting from the replication of one or more sets of chromosomes,
…the additional set of chromosomes is identical to the normal haploid complement of that species.
Autopolyploidy
…can be induced by treating cells with the drug colchicine,
colchicine: is a alkaloid derivative from the autumn crocus (Crocus veneris),
...inhibits microtubule polymerization, and thus inhibits the separation of chromosomes during meiosis.
Colchicine Treatment
• cells undergo S-phase,
• no separation of chromosomes is accomplished,
• no cell division occurs,
• at telophase, the nuclear membrane reforms,
• treatment for one cell cycle leads to 4n cells.
Amphidiploid
…double diploid,
2n1 + 2n2
…have balanced gametes of the type n1 + n2,
these gametes fuse to make fertile 2n1 + 2n2.
Autopolyploidy Applications
• Treating a plant with colchicine often produces autopolyploidy, resulting in plants with larger flowers and/or fruit,
8n 2n4n 2n
Allopolyploidy Applications
B. oleracea (cabbage, cauliflower, Brocolli, kale, etc.)
2n = 18
B. campestris (turnip, turnip rape)
2n = 20
n = 9
n = 10
amphidiploid
n1 + n2 = 19B. napas ( Oil rape, canola oil)2n1 + 2n2 = 38
4n x 2n = 3n?
• The creation of triploids can be accomplished by crossing a tetraploid with a diploid,
• Most triploid individuals are sterile.
Who’d want to Eat That?
• Bananas,
• Seedless Watermelon,
• Most other seedless varieties,
• Some oysters.
Environmental Applications?
grass carp(Ctenopharyngodon idella)
• Triploid grass carp prefer pondweeds,
• do not prefer plants such as cattail, water lily, etc.
Polyploidy Summary
• More than 2 whole sets of chromosomes,
• Autopolyploidy,– from the same genome,– naturally occurring, or induced,– often results in larger varieties,
• Allopolyploidy,– from different genomes,– naturally occurring, or induced,– often results in larger varieties,
• Autotriploids,– most often sterile– can produce beneficial traits.
Monoploid
• male wasps, bees and ants have only 1 haploid genome,
– males develop from unfertilized eggs, • gametes are formed by mitosis.
Monoploid Applications
• monoploid plants can be created by culturing pollen grains (n = 1),
– the population of haploid organisms is then screened for favorable traits,
– the plants are then treated with colchicine which generates a 2n plant homozygous for the favorable traits.
Chromosome Structure
• Changes in chromosome structure can come about due to,
deletions
duplications
rearrangements
Homologous Pairs?
Intercalary
Terminal
Hemizygous
Hemizygous: gene is present in a single dose.
Psuedodominance: hemizygous genes are expressed.
Deletions
…result in partial monosomy,
remember monosomy: 2n, -1,
…the organism is monosomic for the portion of the chromosome that is deleted,
…as in monosomy, most segmental deletions are deleterious.
46, -5p
...terminal deletion of the small arm (petite arm) of chromosome 5,
• Cri-du-chat Syndrome,
– 0.002% live births,
– anatomic mutations,
– often mental retardation,
– abnormal formation of vocal mechanisms.
Chromosomal Duplication
...an event that results in the increase in the number of copies of a particular chromosomal region,
Duplication Cause and Effect
Causes:– duplications often result from unequal crossing over,
– can occur via errors in replication during S-Phase.
Effects:– results in gene redundancy,
– produces phenotypic variation,
– may provide an important source for genetic variability during evolution.
Duplication in Evolution
…essential genes do not tolerate mutation,
…duplications of essential genes, then subsequent mutations, confers adaptive potential to the organism,
…new gene family members are ‘recruited’ to perform new functions.
nutrients
algae
need uptake
transport to other tissue
transport to seeds
moss
need uptake
flowering plant
transport to other tissue
need uptake
Chromosome Structure
• Changes in chromosome structure can come about due to,
deletions
duplications
rearrangements
Chromosomal Inversions
…inversion: aberration in which a portion of the chromosome is turned around 180o.
Paracentric Inversion
...an inversion in which the centomere is not included,
A B C
...a paracentric inversion does not change arm length ratio.
BA CB A
Inversion Heterozygotes
…an organism with one wild-type and one chromosome containing an inversion,
A B C
…not heterozygous for the genes, heterozygous for the chromosomes.
AB C
Dicentric/Ascentric
…results only when the crossing over occurs within the region of the paracentric inversion,
Acentric
…a chromosome having no centromeres,
…segregates to daughter cells randomly, or is lost during cell division,
…deletions impart partial monosomy.
Paracentric Outcomes
1 Normal Gamete, 1 Inversion Gamete, No Crossover Classes
Recombination is not inhibited, but recombinant gametes are selected against.
Pericentric Inversion
...an inversion in which the centromere is included,
A B C
A BC
...a pericentric inversion results in a change in chromosome arm length.
Recombination and Inversions
• Paracentric and Pericentric;
– 1 Normal Gamete,– 1 Inverted Gamete,– No Crossover Classes = No Recombination,
Inversions select against recombinant gametes, thus preserves co-segregation of specific alleles.
Inversions and Evolution
• Inversions ‘lock’ specific alleles together,
– all offspring get the alleles from either a wild-type, or inverted chromosome,
• If the ‘set of alleles’ is advantageous, the set can be maintained in the population.
Assignment
• Understand the differences between ‘Interference’, and the suppression of recombination resulting from inversions,
• Be able to recognize data, and predict results given either case.
Translocations
…translocation: aberration associated with the transfer of a chromosomal segment to a new location in the genome.
Down Syndrome
• 95% of Down Syndrome individuals are a result of Trisomy 21,
– the probability of having a second Down Syndrome child is usually similar to the population at large,
• However, there is second cause of Down Syndrome caused by a Robertsonian translocations that is heritable.
Assignment
• Do a Punnett Square or a Split Fork Diagram of,
Parent 1: wild-type for Chromosomes 14, 21
x
Parent 2: heterozygous for 14q;21q translocation.
Trinucleotide Repeat Expansions
FMR1
Fragile X Mental Retardation 1
cgg
...GCGCGGCGGTGACGGAGGCGCCGCTGCCAGGGGGCGTGCGGCAGCG...
…CTGGGCCTCGAAGCGCCCGCAGCCA
cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cggcgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg
cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cggcgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cggcgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg cgg ... > 200
Assignment(think about these...)
• Truncated Genes;– genes that are no longer full length, due to a
mutation,
• Gene Fusions;– genes that contain coding sequence from two
different genes, resulting from a chromosomal mutation.
Review
• know genotypes and phenotypes,
– trisomy,– monosomy,– inversions,– duplications,– deletions,– fragile site mutations,
• be able to predict heritability, and recognize data-sets and infer the condition.