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Define aneuploidy. How is it different from polyploidy? Describe the individuals having following chromosomal abnormalities. Trisomy of 21st Chromosome XXY XO - Biology

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प्रश्न

Define aneuploidy. How is it different from polyploidy? Describe the individuals having following chromosomal abnormalities.

  1. Trisomy of 21st Chromosome
  2. XXY
  3. XO
दीर्घउत्तर

उत्तर

Failure of segregation of chromatids during cell division cycle results in the gain or loss of a chromosome(s), called aneuploidy.

Difference between aneuploidy and polyploidy

  1. Failure of segregation of chromatids during cell division cycle results in the gain or loss of a chromosome(s), called aneuploidy. Failure of cytokinesis after telophase stage of cell division results in an increase in a whole set of chromosomes in an organism and, this phenomenon is known as polyploidy.
  2. Polyploidy occurs due to altering set of chromosome number such as 2n, 3n, 5n, whereas aneuploidy occurs due to altering particular chromosome or part of a chromosome such as 2n + 1 (trisomic) and 2n – 1 (monosomic).
  3. Aneuploidy can be seen in human as genetic disorders; for example, Tuner syndrome, Klinefelter syndrome and Down syndrome, whereas polyploidy is common in plants.

(a) Down’s Syndrome (Mongolism)

  • The cause of this genetic disorder is the presence of an additional copy of the chromosome number 21 (trisomy of 21) due to non-disjunction of chromosomes during sperm or ova formation.
  • The affected individual is short-statured with small round head, furrowed tongue and partially open mouth. Palm is broad with characteristic palm crease.
  • Physical, psychomotor and mental development is retarded.

(b) Klinefelter’s Syndrome

  • This genetic disorder is also caused due to the presence of an additional copy of X-chromosome resulting into a karyotype of 47, XXY.
  • Such an individual has overall masculine development, however, the feminine development (development of breast, i.e., Gynaecomastia) is also expressed. Such individuals are sterile male.

(c) Turner’s Syndrome Such a disorder is caused due to the absence of one of the X chromosomes, i.e., 45 with XO. Such females are sterile as ovaries are rudimentary besides other features including lack of other secondary sexual characters.

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पाठ 5: Principle of Inheritance and Variation - LONG ANSWER [पृष्ठ ३५]

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एनसीईआरटी एक्झांप्लर Biology [English] Class 12
पाठ 5 Principle of Inheritance and Variation
LONG ANSWER | Q 5. | पृष्ठ ३५

संबंधित प्रश्‍न

Klinefelters’ syndrome is characterized by a karyotype of ____________.


Females with Turners’ syndrome have


Pataus’ syndrome is also referred to as ____________.


Mention the symptoms of Down's syndrome.


Which of the following is not correct?


What is Down’s syndrome? Give its symptoms and cause. Why is it that the chances of having a child with Down’s syndrome increases if the age of the mother exceeds forty years?


How was it concluded that genes are located on chromosomes?


The chromosome number is fixed for all normal organisms leading to species specification whereas any abnormality in the chromosome number of an organism results into abnormal individuals. For example, in humans, 46 is the fixed number of chromosomes both male and female. In males it is '44 + XY' and in females, it is '44 +XX'. Thus the human male is heterogametic, in other words produces two different types of gametes one with '22 + X' chromosomes and the other with '22 + Y' chromosomes respectively. Human female, on the other hand, is homo gametic i.e. produce only one type of gamete with '22 + X' chromosomes only.

Sometimes an error may occur during the meiosis of the cell cycle, where the sister chromatids fail to segregate called nondisjunction, leading to the production of abnormal gametes with altered chromosome numbers. On fertilisation, such gametes develop into abnormal individuals.

(a) State what is aneuploidy. (1)

(b) If during spermatogenesis, the chromatids of sex chromosomes fail to segregate during meiosis, write only the different types of gametes with altered chromosome numbers that could possibly be produced. (1)

(c) A normal human sperm (22 + Y) fertilises an ovum with karyotype '22 +XX'. Name the disorder the offspring thus produced would suffer from and write any two symptoms of the disorder. (2)

OR

(c) Name the best-known and most common autosomal aneuploid abnormality in humans and write any two symptoms. (2)


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