मराठी
कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

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

Advertisements
Advertisements

प्रश्न

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

सविस्तर उत्तर
Advertisements

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.

shaalaa.com
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 5: Principles of Inheritance and Variation - NCERT EXERCISES WITH ANSWERS [पृष्ठ २१२]

APPEARS IN

नूतन Biology [English] Class 12 ISC
पाठ 5 Principles of Inheritance and Variation
NCERT EXERCISES WITH ANSWERS | Q 12. | पृष्ठ २१२

व्हिडिओ ट्यूटोरियलVIEW ALL [1]

संबंधित प्रश्‍न

What is gene pool?


Define the term ‘genome’.


Sketch and label the structure of chromosome.


Describe the structure of chromosomes with a suitable diagram.


Classify the chromosomes on the basis of position of centromere.


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


An allohexaploidy contains


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?


If the haploid number in a cell is 18. The double monosomic and trisomic number will be


Write the salient features of the Sutton and Boveri concept.


Mention the name of man-made cereal. How it is formed?


Identify the scientists who proposed chromosomal theory of inheritance.


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

Which of the following is a primary constriction?


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 ______.


From the following identify the INCORRECT statement/s with respect to the chromosomes.

i. Chromosomes are capable of self replication and play vital role in heredity, mutation, variation, and evolutionary development of eukaryotic species.

ii. Chromosomes are visible during cell division.

iii. Chemically eukaryotic chromosomes are made of mRNA, histone and non-histone proteins.

iv. The number of chromosomes varies within the population of a particular species.


Extra nuclear chromosomes occur in ______.


Extranuclear inheritance is a consequence of presence of genes in ______.


Chromosome maps/genetic maps were first prepared by ______.


What would be the genotype of the parents if the offspring have the phenotypes in 1:1 proportion?


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


What do you mean by locus?


Genes located on same locus but having different expressions are:


Experimental verification of the chromosomal theory of inheritance was done by ______.


Which of the following is sex chromosomal disorder?


A haemophilic man marries a carrier woman and they have a daughter. What is the probability of their daughter being haemophilic?


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.


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×