Tag: molecular basis of inheritance

Questions Related to molecular basis of inheritance

DNA fingerprinting was invented by

  1. Kary Mullis

  2. AIec Jeffery

  3. Dr. Paul Berg

  4. Francis Collins


Correct Option: B
Explanation:

DNA fingerprinting is a forensic technique which identify the individuals by their DNA characteristics. A variable number tandem repeat (or VNTR) refers to presence of a short nucleotide sequence as a tandem repeat on many chromosomes; it exhibit variations in length and number of repeats between individuals. VNTR are 10-100 bp long. This DNA polymorphism is revealed during DNA finger printing in creating DNA profile of individuals. It was invented by AIec Jeffery. The first step in DNA finger printing is extraction of useable DNA followed by its digestion with restriction enzymes to produce the restriction fragments length polymorphisms, or RFLPs. The fragments are sorted according to size by gel electrophoresis. The DNA fragments are then transferred from the gel to the surface of the nylon via southern blotting. For the purpose, the agarose gel is mounted on filter-paper wick and the hybridization membrane is sandwiched between the gel and any absorbent material, which draw the transfer buffer through the gel by capillary action. The buffer flow draw the DNA molecules which are then immobilized on the synthetic membrane. Finally, radioactive probes are washed over the nylon surface to allow their joining to any DNA fragments of same composition.  A photographic film on top of the nylon surface to make a genetic fingerprint. 

DNA finger printing technique was discovered by 

  1. Wilmut

  2. A. Jeffreys

  3. Eithoven

  4. Kary Mullis


Correct Option: B
Explanation:

DNA finger printing is a forensic technique which identifies the individuals by their DNA characteristics. A variable number tandem repeat (or VNTR) refers to the presence of a short nucleotide sequence as a tandem repeat on many chromosomes; it exhibits variations in length and number of repeats between individuals. VNTR are 10-100 bp long. This DNA polymorphism is revealed during DNA finger printing in creating DNA profile of individuals.  It was invented by AIec Jeffreys. The first step in DNA finger printing is the extraction of usable DNA followed by its digestion with restriction enzymes to produce the restriction fragments length polymorphisms or RFLPs. The fragments are then sorted according to size by gel electrophoresis. The sorted DNA fragments are then transferred from the gel to the surface of the nylon via southern blotting. For the purpose, the agarose gel is mounted on filter paper wick and the hybridization membrane is sandwiched between the gel and any absorbent material, which draw the transfer buffer through the gel by capillary action. The buffer flow draws the DNA molecules which are then immobilized on the synthetic membrane. Finally, radioactive probes are washed over the nylon surface to allow their joining to any DNA fragments of same composition. A photographic film on top of the nylon surface to make a genetic fingerprint. 

Which of the following tests helps to solve crimes?

  1. Proteomics

  2. DNA fingerprinting

  3. Blood analysis

  4. None of the above


Correct Option: B
Explanation:

DNA fingerprinting is a test which is used to identify and evaluate the genetic information called as DNA in a person's cells. It is called as a "fingerprint" because it is very unlikely that any two people would have exactly the same DNA information, in the same way that it is very unlikely that any two people would have exactly the same physical fingerprint. The test is used to determine whether a family relationship exists between two people, to identify organisms causing a disease and to solve crimes. 

Which of the following scientist has developed the technique DNA fingerprinting?

  1. Watson and Crick

  2. Yamanaka

  3. Alec Jeffrey

  4. Paul Berg


Correct Option: C

Centre of DNA Fingerprinting and Diagnostics (CDFD) is located at

  1. Delhi

  2. Chennai

  3. Kolkata

  4. Hyderabad


Correct Option: D

Which out of the following statements is incorrect?

  1. Genetic code is ambiguous.

  2. Genetic code is degenerate.

  3. Genetic code is universal.

  4. Genetic code is non-overlapping.


Correct Option: A
Explanation:

Since there are 64 triplet codons and only 20 amino acids, genetic code is non-ambiguous. Non-ambiguous code means that there is no ambiguity about a particular code. One codon specifies only one amino acid and not any other except GUG which normally codes for valine but in certain conditions it also codes for N-formyl methionine as initiation codon.

Choose the correct answer from the alternatives given, Human genome consists of approximately

  1. $3 \, \times \, 10^9$ bp

  2. $6 \, \times \, 10^9$ bp

  3. 20,000 + 25,000 bp

  4. $2.2 \, \times \, 10^4$ bp


Correct Option: A
Explanation:
The human genome contains 23 chromosomes. The DNA in the haploid set contains 3 billion base pairs.
So, the correct answer is '($3\, \times \,10^9$ bp)'

Choose the correct answer from the alternatives given :
Which of the following statements regarding human genome is incorrect?

  1. Human genome consists of $3 \, \times \, 10^9$ bp and about 20,500 genes.

  2. The average gene size is 3000 bop and dystrophin is the largest known human gene.

  3. Chromosome 1 contains maximum (2968) number of genes and Y-chrbmosome has the least (231) number of genes.

  4. Repeated (or repetitive) sequences are not present in human genome.


Correct Option: D
Explanation:

Repeated or repetitive sequences make up large portion of human genome. Repetitive sequences are nucleotide sequences that are repeated many times, sometimes hundred to thousand times. They have no direct coding function but provide information as to chromosome structure, dynamics and evolution. Approximately 1 million copies of short 5-8 base pair repeated sequences are clustered around centromeres and near the ends of chromosomes. They represent junk DNA. 

So, the correct answer is 'Repeated (or repetitive) sequences are not present in human genome'.

All living organism present past and future are 

  1. Not linked to any extent

  2. Linked to one another in their cell membrane

  3. Linked to one another by the sharing of the common genetic materials ,but to varying degrees

  4. Linked to another by the sharing of the common genetic material to $100\%$ extent


Correct Option: C
Explanation:

All living organisms—present, past and future are linked to one another by the sharing of the common genetic material, but to varying degrees.

The genetic material of living organisms undergoes mutations and reshuffling of genes. This causes variations in the genetic material. Variations are so abundant that no two individuals of the same race are exactly similar.
So the answer is 'Linked to one another by the sharing of the common genetic materials, but to varying degrees'. 

Which of the following is an application  of human genome project?

  1. Understanding of phylogenetic disorder

  2. Improvement in gene therapy

  3. Understanding of mutation concept

  4. All of the above


Correct Option: D