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प्रश्न
Briefly mention the contribution of T. H. Morgan in genetics.
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उत्तर
Thomas Hunt Morgan (1866–1945), an American geneticist and Nobel Prize winner in 1933, is recognised as the “Father of Experimental Genetics” for his work on and discovery of linkage, crossing over, sex linkage, criss-cross inheritance, linkage maps, gene mutability, and so on. He is known as the fly man of genetics because he used fruit flies (Drosophila melanogaster) as research subjects in experimental genetics. His book “The Theory of Gene” primarily acknowledged genetics as a unique discipline of biology. In 1910, he identified linkage and discriminated between linked and unlinked genes. Morgan and Castle’s (1911) “Chromosomal Theory of Linkage” argued that genes are located on chromosomes and ordered in linear order. Morgan and Sturtevant (1911) discovered that the frequency of crossover (recombination) between two connected genes is exactly proportional to their distance. 1% recombination is equivalent to 1 centi Morgan (cM) or 1 map unit. He researched sex-linked inheritance and discovered a white-eyed male Drosophila in a red-eyed population, proving that the gene for eye colour is located on the X chromosome. The man passed genes on X chromosomes to the daughter, whereas the son receives genes on X chromosomes from the mother. It is known as criss-cross inheritance.
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संबंधित प्रश्न
If centromere is situated in the middle of the chromosome, it is called ________.
(a) Metacentric
(b) Acrocentric
(c) Submetacentric
(d) Telocentric
If the number of chromosomes in an endosperm cell is 27, what will be the chromosome number in the definitive nucleus?
- 9
- 18
- 27
- 36
Define the term ‘genome’.
Sketch and label the structure of chromosome.
A male honeybee has 16 chromosomes whereas its female has 32 chromosomes. Give one reason.
Who had proposed the chromosomal theory of inheritance?
Explain the types of chromosomes on the basis of position of centromere.
Name the type of cell division involved in the production of sperms by honey bees.
Classify the chromosomes on the basis of position of centromere.
Choose the correct options of the following question:
Study the given monohybrid cross:

A test cross for this Fj will be:
Define the Homologous chromosomes
Answer the following question.
Compare in any three ways the chromosomal theory of inheritance as proposed by Sutton and Bovery with that of experimental results on pea plant presented by Mendel.
Telocentric chromosome differs from acrocentric chromosome in that ____________.
Read the following statements regarding 'X and Y' chromosomes and select the correct option.
P - Due to presence of large amount of euchrornatin X chromosome is genetically more active.
Q - Due to presence of small amount of heterochromatin Y chromosome is genetically more active.
During cell division, spindle fibres get attached to the disc shaped structures present on the centromere are known as ______.
At secondary constriction I, ______ becomes organized during interphase.
Which of the following does NOT agree with chrotnosomal theory of inheritance?
A plant having the genotype AABbCC will produce ______ kinds of gametes.
Two or more independent genes present on different chromosomes which determine nearly same phenotype are called ______.
Which three scientists independently rediscovered Mendel’s work?
How many types of gametes would be produced if the genotype of a parent is AaBB?
Which of the following statements indicates parallelism in genes and chromosomes?
- They occur in pairs.
- They segregate during gamete formation.
- They show linkage.
- Independent pairs segregate independently.
A couple has two daughters. What is the probability that the third child will also be a female?
Which of the following sentences are correct?
1. The offspring exhibit only parental combinations due to incomplete linkage
2. The linked genes exhibit some crossing over in complete linkage
3. The separation of two linked genes are possible in incomplete linkage
4. Crossing over is absent in complete linkage
Which of the following is sex chromosomal disorder?
