TLS Online TPP Program

#Question id: 339


The edges of each base pair are exposed in the major and minor grooves, creating a pattern of hydrogen-bond donors and acceptors and of hydrophobic groups (allowing for Vander Waals interactions) that identifies the base pair. The edge of an C : G base pair displays the following chemical groups in the following order in the major groove:

#Unit 1. Molecules and their Interaction Relevant to Biology
  1. A hydrogen-bond acceptor (at N7 of guanine), a hydrogen-bond acceptor (the carbonyl on C6 of guanine), a hydrogen-bond donor (the exocyclic amino group on C3 of cytosine), and a small nonpolar hydrogen (the hydrogen at C5 of cytosine)

  2. A hydrogen-bond acceptor (at N7 of guanine), a hydrogen-bond acceptor (the carbonyl on C6 of guanine), a hydrogen-bond donor (the exocyclic amino group on C4 of cytosine), and a small nonpolar hydrogen (the hydrogen at C5 of cytosine)

  3. A small nonpolar hydrogen (the hydrogen at C5 of cytosine), a hydrogen-bond donor (the exocyclic amino group on C4 of cytosine), a hydrogen-bond acceptor (the carbonyl on C6 of guanine) and a hydrogen-bond acceptor (at N7 of guanine)

  4. A small nonpolar hydrogen (the hydrogen at C5 of cytosine), a hydrogen-bond acceptor (the exocyclic amino group on C4 of cytosine), a hydrogen-bond acceptor (the carbonyl on C6 of guanine) and a hydrogen-bond donor (at N7 of guanine)

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TLS Online TPP Program

#Question id: 13080

#Unit 13. Methods in Biology

In RAPDs amplification will take place only of those regions of the genome that have the 

TLS Online TPP Program

#Question id: 13081

#Unit 13. Methods in Biology

Correct statements about RAPD’s
A. RAPD polymorphism is detected by using oligonucleotides usually more than 10 bases long of random sequences as primers in a reaction.
B. In a strain which has in genomic DNA sequences complementary to the primer oligonucleotide, PCR products will be detected in the gel,
C. Typical RAPD markers show limited variation between parents, especially in naturally inbreeding species.
D. RAPDs are more sensitive than RFLPs to experimental conditions making them more difficult to be consistent and reproducible.

TLS Online TPP Program

#Question id: 13082

#Unit 13. Methods in Biology

Statement: AFLP shares some features of both RFLP and RAPD analyses.
Explanations: I. It uses restriction enzyme-digested genomic DNA as template for PCR amplification using primers that contain the restriction enzyme recognition sites plus a number of, usually 2-3, arbitrary nucleotides.
II. AFLPs are faster, less labour intensive and provide more information than RFLPs, and they are highly reproducible, which is a great advantage over RAPDs.

TLS Online TPP Program

#Question id: 13083

#Unit 13. Methods in Biology

The genomic DNA of an organism is digested with two restriction enzymes; one of the, PstI (CTGCA/G), while the other., MseI (T/TAA). This would generate the following 3 types of DNA fragments: 
(1) both ends cleaved by PstI (Pst-Pst), 
(2) both ends cleaved by MseI (Mse-Mse), and 
(3) one end generated by each of the two enzymes (Pst-Mse). 
the most frequent fragments in decreasing order,

TLS Online TPP Program

#Question id: 13084

#Unit 13. Methods in Biology

Statement: In a modified version of AFLP, the selection of fragments using biotin-streptavidin binding is avoided.
Explanations: I. The fragments are ligated to the appropriate adapters and used for PCR amplification using two AFLP primers, each primer having a single selection nucleotide; this is called preamplification step.
II. The PCR products from this preamplificated step are diluted and used as template for second PCR amplification.

TLS Online TPP Program

#Question id: 13085

#Unit 13. Methods in Biology

The most common microsatellite sequence encountered in human genome is the sequence