A species of plant (species 1) is diploid (2n = 6) with chromosomes AABBCC and a related species (species 2) is also diploid (2n = 4) with chromosomes PPQQ. The following statements were given by students regarding the chromosome numbers involving these plant species: A. Autotriploid of species 1 will have 12 chromosomes B. Allotetraploid involving species 1 and 2 will have 16 chromosomes C. A monosomy in species 1 will generate 5 chromosomes D. A double trisomy in species 1 will generate 8 chromosomes E. A nullisomy in species 2 will generate 2 chromosomes The combination of statements with all correct answers is:
C, D and E
Let's analyze the chromosome numbers for the given plant species and the different ploidy and aneuploidy conditions described in the statements.
We are given two plant species:
An autotriploid arises from a single species where the chromosome number is tripled ($\text{3n}$).
For Species 1, the haploid number ($\text{n}$) is $\text{3}$.
An autotriploid of Species 1 would have $\text{3} \times \text{n} = \text{3} \times \text{3} = \text{9}$ chromosomes.
Statement A says an autotriploid of species 1 will have $\text{12}$ chromosomes. This is incorrect.
An allotetraploid is formed by combining the complete diploid sets of two different species. It can be represented as $\text{2n}_1 + \text{2n}_2$ or $\text{2(n}_1 + \text{n}_2)$.
Diploid number for Species 1 ($\text{2n}_1$) is $\text{6}$.
Diploid number for Species 2 ($\text{2n}_2$) is $\text{4}$.
An allotetraploid involving Species 1 and 2 would have $\text{2n}_1 + \text{2n}_2 = \text{6} + \text{4} = \text{10}$ chromosomes.
Alternatively, the hybrid ($\text{n}_1 + \text{n}_2$) would have $\text{3} + \text{2} = \text{5}$ chromosomes. Doubling this gives $\text{2} \times \text{5} = \text{10}$ chromosomes.
Statement B says an allotetraploid involving species 1 and 2 will have $\text{16}$ chromosomes. This is incorrect.
Monosomy is a type of aneuploidy where a single chromosome is missing from a diploid set. The chromosome number is $\text{2n} - \text{1}$.
Diploid number for Species 1 ($\text{2n}$) is $\text{6}$.
A monosomy in Species 1 would have $\text{2n} - \text{1} = \text{6} - \text{1} = \text{5}$ chromosomes.
Statement C says a monosomy in species 1 will generate $\text{5}$ chromosomes. This is correct.
Trisomy is a type of aneuploidy where there is an extra copy of a single chromosome, resulting in $\text{2n} + \text{1}$.
Double trisomy means there are extra copies of two different chromosomes, resulting in $\text{2n} + \text{1} + \text{1}$.
Diploid number for Species 1 ($\text{2n}$) is $\text{6}$.
A double trisomy in Species 1 would have $\text{2n} + \text{1} + \text{1} = \text{6} + \text{2} = \text{8}$ chromosomes.
Statement D says a double trisomy in species 1 will generate $\text{8}$ chromosomes. This is correct.
Nullisomy is a type of aneuploidy where a pair of homologous chromosomes is missing from a diploid set. The chromosome number is $\text{2n} - \text{2}$.
Diploid number for Species 2 ($\text{2n}$) is $\text{4}$.
A nullisomy in Species 2 would have $\text{2n} - \text{2} = \text{4} - \text{2} = \text{2}$ chromosomes.
Statement E says a nullisomy in species 2 will generate $\text{2}$ chromosomes. This is correct.
The statements with all correct answers are C, D, and E.
Fertilization of gametes containing chromosome with duplications or deletions often results in children with disabilities. What is the probability of a couple where the male is karyotypically normal and the female has a pericentric inversion in heterozygous condition producing a child with disabilities if crossing over took place within the pericentric inversion in 26% of meiotic divisions?
In this case consider that fertilization with a gamete containing chromosomes with duplications or deletion will result in disabilities.
Chromosomal inversions are balanced rearrangements and thus do not change the overall amount of genetic material. While inversions can exist in homozygous condition, some only exist as heterozygotes. In the latter condition, the breakpoint disrupts:
A colour blind father has a daughter who is also colour blind and has Turner's syndrome. The genotype of the daughter is due to:
A cruciform structure of chromosomes during meiosis is a characteristic feature of:
If a gamete produced following non disjunction of a chromosome at second meiotic division was fertilized by a normal gamete, what is the expected frequency of trisomic progeny?