Okazaki Fragments
Trending Questions
Match the RNA polymerase types in column I with that of the product they synthesize in column II.
Column I | Column II |
a. RNA pol. I | i. Synthesizes mRNA and hnRNA |
b. RNA pol. II | ii. Synthesizes tRNA , 5 srRNA, Sn RNA in nucleolus |
c. RNA pol. III | iii. Synthesizes rRNA (28S, 18S) in nucleolus |
a- i, b – ii, c - iii
- a – ii, b – iii, c – i
- a – iii, b – i, c – ii
- a – iii, b – ii, c – i
What is the unit of replication?
- GC region
- parental strand
- origin of replication or (ORI)
- daughter strand
I. If a linear DNA molecule is digested with a restriction enzyme at four recognition sites, 4 fragments would be produced.
II. If a closed circular DNA molecule is digested with a restriction enzyme at six recognition sites, 6 fragments would be produced.
III. If a linear DNA molecule is digested with a restriction enzyme at four recognition sites on the DNA, 5 fragments would be produced.
IV. If a closed circular DNA molecule is digested with a restriction enzyme at six recognition sites, 7 fragments would be produced.
- 1
- 2
- 3
- 4
Why do we need PCR primers?
An Okazaki fragment includes:
Only short fragments of deoxyribonucleotides
Only short RNA fragments
RNA primer + short fragments of deoxyribonucleotides
Only RNA primer
- they cleave both strands of DNA so as to leave no unpaired bases on either end
- they make staggered cuts on the two DNA strands leaving two to four nucleotides of one strand unpaired
- they cut the methylated strand of host DNA by error
- enzymatic digestion of DNA strand leave unpaired bases on both ends of the two strands
- synthesizes DNA
- cuts the DNA molecule randomly
- cuts the DNA molecule at specific sites
- restricts the synthesis of DNA inside the nucleus
- Origin
- Initiation point
- Primer
- Replication fork
(A) BamHI and EcoRI have five and six base pair long recognition sequences, respectively.
(B) Roman number in the restriction enzyme name indicates the order in which it was isolated from the bacteria.
(C) Restriction endonuclease function by inspecting the length of a DNA molecule for recognition sequences.
(D) The palindrome in DNA reads the same on the two strands when orientation is kept the same.
Choose the correct option.
- A, B, C
- B and C only
- B, C, D
- All of the above
- Poly (A) tail sequences
- Degenerate primer sequence
- Okazaki sequences
- Palindromic Nucleotide sequences
- In capping, nucleotide methyl cytosine triphosphate is added to 5’ end of hnRNA
- RNA splicing is the removal of exons and joining of introns
- 5S rRNA is transcribed by RNA polymerase I
- Tailing at 3’ end of RNA is a template-independent process
- 5’ GAATTC 3’
- 5’ GGATCC 3’
- 5’ AAGCTT 3’
- 5’ CAGCTG 3’
- 3′→5′
- 5′→3′
- 5′→5′
- 3′→3′
I. It is isolated from Escherichia coli RY13.
II. Its recognition sequence is
5' GAATTC 3'
3' CTTAAG 5'
III. It produces complementary blunt ends.
IV. It was the first restriction endonuclease to be characterised.
- I and II
- II and IV
- III and IV
- I and IV
During DNA replication, the lagging strand gets copied as short segments of 100-200 base pairs in length, which are known as
Okazaki fragments
Ori site
RNA primers
Replication fork
- Leading strand
- Lagging strand
- Sense strand
- None of the above
- Drosophila melanogaster
- Streptococcus pneumoniae
- Salmonella typhimurium
- Escherichia coli
An Okazaki fragment includes
Only short fragments of deoxyribonucleotides
Only short RNA fragments
RNA primer + short fragments of deoxyribonucleotides
Only RNA primer
- GC region
- parental strand
- origin of replication or (ORI)
- daughter strand
- 2000
- 200
- 1000
- 20
- The leading strand towards replication fork
- The lagging strand towards replication fork
- The leading strand away from replication fork
- The lagging strand away from replication fork
I. It is isolated from Escherichia coli RY13.
II. Its recognition sequence is
5' GAATTC 3'
3' CTTAAG 5'
III. It produces complementary blunt ends.
IV. It was the first restriction endonuclease to be characterised.
- I and II
- II and IV
- III and IV
- I and IV
I. If a linear DNA molecule is digested with a restriction enzyme at four recognition sites, 4 fragments would be produced.
II. If a closed circular DNA molecule is digested with a restriction enzyme at six recognition sites, 6 fragments would be produced.
III. If a linear DNA molecule is digested with a restriction enzyme at four recognition sites on the DNA, 5 fragments would be produced.
IV. If a closed circular DNA molecule is digested with a restriction enzyme at six recognition sites, 7 fragments would be produced.
- 1
- 2
- 3
- 4
- 3.4 ˚A
- 20.0 ˚A
- 34.0 ˚A
- 3.04 ˚A
An Okazaki fragment includes
Only short fragments of deoxyribonucleotides
Only short RNA fragments
RNA primer + short fragments of deoxyribonucleotides
Only RNA primer