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Briefly mention the contribution of T. H. Morgan in genetics.

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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 recognised genetics as a distinct discipline within 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 a 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 the X chromosome to the daughter, whereas the son received genes on the X chromosome from the mother. It is known as criss-cross inheritance.

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अध्याय 4: Principles of Inheritance and Variation - EXERCISES [पृष्ठ ७८]

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एनसीईआरटी Biology [English] Class 12
अध्याय 4 Principles of Inheritance and Variation
EXERCISES | Q 9. | पृष्ठ ७८
नूतन Biology [English] Class 12 ISC
अध्याय 4 Principles of Inheritance and Variation
NCERT EXERCISES WITH ANSWERS | Q 12. | पृष्ठ २१२

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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


Define the term ‘genome’.


State the difference between meiocyte and gamete with respect to chromosome number.


Explain the types of chromosomes on the basis of position of centromere.


Classify the chromosomes on the basis of position of centromere.


Define the Homologous chromosomes


Short Answer Question.

Explain the chromosomal theory of inheritance.


Explain codominance in colour coat in cattle with checker board method.


The A and B genes are 10 cm apart on a chromosome. If an AB/ab heterozygote is test crossed to ab/ab, how many of each progeny class would you expect out of 100 total progeny?


Write the salient features of the Sutton and Boveri concept.


When two different genes came from the same parent they tend to remain together.

Write the observed phenotypic ratio.


Match the column I (Type of chromosome) with column II (name of chromosome).

  Type of chromosome   Name of chromosome
i. P. Acrocentric
ii. Q. Telocentric
iii. R. Metacentric
iv. S. Sub-metacentric

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.


Identify the term that represents the degree of repetition of the primary basic number of chromosomes in a cell.


Extranuclear inheritance occurs in ______.


Extra nuclear chromosomes occur in ______.


In a certain taxon of insects some have 17 chromosomes and the others have 18 chromosomes. The 17 and 18 chromosome-bearing organisms are ______.


Mendel’s work was rediscovered by three scientists in the year ______.


Chromosome maps/genetic maps were first prepared by ______.


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?

  1. They occur in pairs.
  2. They segregate during gamete formation.
  3. They show linkage.
  4. Independent pairs segregate independently.

A couple has two daughters. What is the probability that the third child will also be a female?


During mitosis, chromosomes distribution to the daughter cell is ______.


Genes located on same locus but having different expressions are:


How do genes and chromosomes share similarity from the point of view of genetical studies?


Which of the following is sex chromosomal disorder?


Consider the following information and answer the question that follows:

  • Reshma’s mother is normal, but her father is suffering from PKU.
  • Reshma is suffering from PKU. She has two younger brothers who are identical twins; both are suffering from PKU. Reshma’s two elder sisters are normal.
  • Reshma marries Robert, who is normal. Reshma gives birth to a son named Jason who is normal. After some time, Reshma and Robert have two more children: a daughter with symptoms of PKU and a son without any symptoms of PKU.

Make a single pedigree chart using the above information to show the pattern of inheritance of phenylketonuria (PKU) in the family of Reshma.


According to the Chromosomal Theory of Inheritance, chromosomes serve which fundamental role in heredity?


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