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MCQ MOLECULAR BASIS
1.
According to the Double-Helix model of DNA proposed by James Watsonand Francis Crick (1953), what is the pitch of the right-handed DNA helix
and the approximate distance between two consecutive base pairs?
(A) Pitch = 0.34 nm; Distance per bp = 3.4 nm
(B) Pitch = 3.4 nm; Distance per bp = 0.34 nm
(C) Pitch = 20 nm; Distance per bp = 2.0 nm
(D) Pitch = 34 nm; Distance per bp = 3.4 nm
2.
According to the Double-Helix model of DNA proposed by James Watsonand Francis Crick (1953), what is the pitch of the right-handed DNA helix
and the approximate distance between two consecutive base pairs?
(A) Pitch = 0.34 nm; Distance per bp = 3.4 nm
(B) Pitch = 3.4 nm; Distance per bp = 0.34 nm
(C) Pitch = 20 nm; Distance per bp = 2.0 nm
(D) Pitch = 34 nm; Distance per bp = 3.4 nm
3.
In eukaryotic chromatin packaging, histones are positively charged basicproteins that organize into a histone octamer because they are rich in which
pair of basic amino acid residues carrying positive charges in their side
chains?
(A) Valine and Glutamic acid
(B) Lysine and Arginine
(C) Methionine and Tryptophan
(D) Serine and Tyrosine
4.
In eukaryotic chromatin packaging, histones are positively charged basicproteins that organize into a histone octamer because they are rich in which
pair of basic amino acid residues carrying positive charges in their side
chains?
(A) Valine and Glutamic acid
(B) Lysine and Arginine
(C) Methionine and Tryptophan
(D) Serine and Tyrosine
5.
How many base pairs (bp) of negatively charged DNA helix are wrappedaround a single positively charged histone octamer to form a typical
eukaryotic nucleosome?
(A) 100 bp
(B) 146 bp
(C) 200 bp
(D) 400 bp
6.
How many base pairs (bp) of negatively charged DNA helix are wrappedaround a single positively charged histone octamer to form a typical
eukaryotic nucleosome?
(A) 100 bp
(B) 146 bp
(C) 200 bp
(D) 400 bp
7.
In a typical eukaryotic interphase nucleus, the region of chromatin that isloosely packed, stains light, and is transcriptionally active is termed:
(A) Heterochromatin
(B) Nucleoid
(C) Euchromatin
(D) Satellite DNA
8.
In a typical eukaryotic interphase nucleus, the region of chromatin that isloosely packed, stains light, and is transcriptionally active is termed:
(A) Heterochromatin
(B) Nucleoid
(C) Euchromatin
(D) Satellite DNA
9.
Which of the following statements regarding the Meselson and Stahl (1958)experiment on Escherichia coli is INCORRECT?
(A) 15N is a radioactive isotope of nitrogen that emits beta particles during
decay.
(B) 15N-DNA can be separated from 14N-DNA only based on densities in a CsCl
gradient.
(C) DNA extracted 20 minutes after transfer from 15N to 14N medium had an
intermediate/hybrid density.
(D) DNA extracted after 40 minutes (II generation) was composed of equal
amounts of hybrid and light DNA.
10.
Which of the following statements regarding the Meselson and Stahl (1958)experiment on Escherichia coli is INCORRECT?
(A) 15N is a radioactive isotope of nitrogen that emits beta particles during
decay.
(B) 15N-DNA can be separated from 14N-DNA only based on densities in a CsCl
gradient.
(C) DNA extracted 20 minutes after transfer from 15N to 14N medium had an
intermediate/hybrid density.
(D) DNA extracted after 40 minutes (II generation) was composed of equal
amounts of hybrid and light DNA.
11.
The haploid content of human DNA isapproximately
(A) 4.6 × 106 bp
(B) 6.6 × 109 bp
(C) 3.3 × 109 bp
(D) 5386 bp
12.
The haploid content of human DNA isapproximately
(A) 4.6 × 106 bp
(B) 6.6 × 109 bp
(C) 3.3 × 109 bp
(D) 5386 bp
13.
A nitrogenous base is linked to the pentose sugar to form anucleoside through
(A) a 3′-5′ phosphodiester linkage
(B) a peptide linkage at 2′ carbon
(C) a phosphoester linkage at 5′ carbon
(D) an N-glycosidic linkage at 1′ carbon
14.
A nitrogenous base is linked to the pentose sugar to form anucleoside through
(A) a 3′-5′ phosphodiester linkage
(B) a peptide linkage at 2′ carbon
(C) a phosphoester linkage at 5′ carbon
(D) an N-glycosidic linkage at 1′ carbon
15.
A nucleotide is formed when a phosphate group is linked to the OHof the ______ carbon of a nucleoside through a ______ linkage.
(A) 5′ ; phosphoester
(B) 3′ ; phosphodiester
(C) 1′ ; N-glycosidic
(D) 2′ ; phosphoester
16.
A nucleotide is formed when a phosphate group is linked to the OHof the ______ carbon of a nucleoside through a ______ linkage.
(A) 5′ ; phosphoester
(B) 3′ ; phosphodiester
(C) 1′ ; N-glycosidic
(D) 2′ ; phosphoester
17.
The chemical name of thymine , found in DNA in place of thebase uracil of RNA, is
(A) 5-methyl uracil
(B) 2-amino adenine
(C) 5-methyl cytosine
(D) 6-amino purine
18.
The chemical name of thymine , found in DNA in place of thebase uracil of RNA, is
(A) 5-methyl uracil
(B) 2-amino adenine
(C) 5-methyl cytosine
(D) 6-amino purine
19.
According to the observation of Erwin Chargaff , in a double strandedDNA the ratios between
(A) A and G, and between T and C, are equal to one
(B) A and C, and between T and G, are equal to one
(C) A and T, and between G and C, are equal to one
(D) purines and phosphates are equal to one
20.
According to the observation of Erwin Chargaff , in a double strandedDNA the ratios between
(A) A and G, and between T and C, are equal to one
(B) A and C, and between T and G, are equal to one
(C) A and T, and between G and C, are equal to one
(D) purines and phosphates are equal to one
21.
The number of hydrogen bonds between A and T and between Gand C in a DNA double helix respectively
are
(A) 3 and 2
(B) 2 and 2
(C) 3 and 3
(D) 2 and 3
22.
The number of hydrogen bonds between A and T and between Gand C in a DNA double helix respectively
are
(A) 3 and 2
(B) 2 and 2
(C) 3 and 3
(D) 2 and 3
23.
Histones are rich in the basic amino acid residues(A) aspartic acid and glutamic acid
(B) glycine and alanine
(C) cysteine and methionine
(D) lysine and arginine
24.
Histones are rich in the basic amino acid residues(A) aspartic acid and glutamic acid
(B) glycine and alanine
(C) cysteine and methionine
(D) lysine and arginine
25.
The region of chromatin that is loosely packed, stains light and issaid to be transcriptionally active is called
(A) heterochromatin
(B) nucleoid
(C) euchromatin
(D) centromere
26.
The region of chromatin that is loosely packed, stains light and issaid to be transcriptionally active is called
(A) heterochromatin
(B) nucleoid
(C) euchromatin
(D) centromere
27.
In 1928, Frederick Griffith injected a mixture of heat-killed S strainand live R strain Streptococcus pneumoniae into mice. The result
was that the mice
(A) lived and no bacteria were recovered
(B) lived and only R bacteria were recovered
(C) died and living S bacteria were recovered
(D) died and only R bacteria were recovered
28.
In 1928, Frederick Griffith injected a mixture of heat-killed S strainand live R strain Streptococcus pneumoniae into mice. The result
was that the mice
(A) lived and no bacteria were recovered
(B) lived and only R bacteria were recovered
(C) died and living S bacteria were recovered
(D) died and only R bacteria were recovered
29.
In the experiments of Avery, MacLeod and McCarty, transformationof R cells into S cells was inhibited by
digestion with
(A) protease
(B) RNase
(C) DNAs
(D) DNase
30.
In the experiments of Avery, MacLeod and McCarty, transformationof R cells into S cells was inhibited by
digestion with
(A) protease
(B) RNase
(C) DNAs
(D) DNase
31.
Hershey and Chase (1952) labelled the DNA of bacteriophageswith radioactive ______ and the protein coat with radioactive
______.
(A) sulfur; phosphorus
(B) phosphorus; sulfur
(C) nitrogen; carbon
(D) phosphorus; nitrogen
32.
Hershey and Chase (1952) labelled the DNA of bacteriophageswith radioactive ______ and the protein coat with radioactive
______.
(A) sulfur; phosphorus
(B) phosphorus; sulfur
(C) nitrogen; carbon
(D) phosphorus; nitrogen
33.
RNA is labile and easily degradable , whereas DNA is chemicallymore stable, mainly because every
nucleotide in RNA has a reactive
(A) 3′-phosphate group
(B) 2′-OH group
(C) 5-methyl group
(D) N-glycosidic bond
34.
RNA is labile and easily degradable , whereas DNA is chemicallymore stable, mainly because every
nucleotide in RNA has a reactive
(A) 3′-phosphate group
(B) 2′-OH group
(C) 5-methyl group
(D) N-glycosidic bond
35.
The scheme in which the two strands separate and each acts as atemplate so that every daughter DNA has
one parental and one newly synthesised strand is called ______
replication.
(A) conservative
(B) dispersive
(C) semiconservative
(D) continuous
36.
The scheme in which the two strands separate and each acts as atemplate so that every daughter DNA has
one parental and one newly synthesised strand is called ______
replication.
(A) conservative
(B) dispersive
(C) semiconservative
(D) continuous
37.
E. coli grown for many generations in 15NH4Cl medium wastransferred to 14NH4Cl medium. The DNA extracted after one
generation (20 minutes) , when centrifuged in a CsCl
density gradient, showed
(A) only heavy DNA
(B) only light DNA
(C) equal amounts of heavy and light DNA
(D) only hybrid (intermediate density) DNA
38.
E. coli grown for many generations in 15NH4Cl medium wastransferred to 14NH4Cl medium. The DNA extracted after one
generation (20 minutes) , when centrifuged in a CsCl
density gradient, showed
(A) only heavy DNA
(B) only light DNA
(C) equal amounts of heavy and light DNA
(D) only hybrid (intermediate density) DNA
39.
DNA-dependent DNA polymerases catalyse polymerisation ofdeoxynucleotides only in the direction
(A) 3′ → 5′
(B) 5′ → 3′
(C) both 5′ → 3′ and 3′ → 5′
(D) 5′ → 5′
40.
DNA-dependent DNA polymerases catalyse polymerisation ofdeoxynucleotides only in the direction
(A) 3′ → 5′
(B) 5′ → 3′
(C) both 5′ → 3′ and 3′ → 5′
(D) 5′ → 5′
41.
In eukaryotes, DNA replication takes place in the ______ ofthe cell cycle, and a failure of cell division after DNA
replication results in
(A) G1-phase; aneuploidy
(B) M-phase; polyploidy
(C) S-phase; polyploidy
(D) G2-phase; monosomy
42.
In eukaryotes, DNA replication takes place in the ______ ofthe cell cycle, and a failure of cell division after DNA
replication results in
(A) G1-phase; aneuploidy
(B) M-phase; polyploidy
(C) S-phase; polyploidy
(D) G2-phase; monosomy
43.
The figure shows a short polynucleotide chain with four structural featurespointed by the letters P, Q, R and S.
Identify the correct match.
(A) P: free 5′ phosphate; Q: free 3′ OH; R: nitrogenous base; S: pentose sugar
(B) P: free 3′ OH; Q: free 5′ phosphate; R: pentose sugar; S: nitrogenous base
(C) P: nitrogenous base; Q: pentose sugar; R: free 5′ phosphate; S: free 3′ OH
(D) P: pentose sugar; Q: free 5′ phosphate; R: free 3′ OH; S: nitrogenous base
44.
The figure shows a short polynucleotide chain with four structural featurespointed by the letters P, Q, R and S.
Identify the correct match.
(A) P: free 5′ phosphate; Q: free 3′ OH; R: nitrogenous base; S: pentose sugar
(B) P: free 3′ OH; Q: free 5′ phosphate; R: pentose sugar; S: nitrogenous base
(C) P: nitrogenous base; Q: pentose sugar; R: free 5′ phosphate; S: free 3′ OH
(D) P: pentose sugar; Q: free 5′ phosphate; R: free 3′ OH; S: nitrogenous base
45.
In the diagram of a nucleosome, the parts marked X, Y and Z are respectively(A) X: DNA; Y: histone octamer; Z: H1 histone
(B) X: histone octamer; Y: DNA; Z: H1 histone
(C) X: H1 histone; Y: DNA; Z: histone octamer
(D) X: DNA; Y: H1 histone; Z: histone octamer
46.
In the diagram of a nucleosome, the parts marked X, Y and Z are respectively(A) X: DNA; Y: histone octamer; Z: H1 histone
(B) X: histone octamer; Y: DNA; Z: H1 histone
(C) X: H1 histone; Y: DNA; Z: histone octamer
(D) X: DNA; Y: H1 histone; Z: histone octamer
47.
A transcription unit in DNA is defined primarily by three regions,namely
(A) exon, intron and promoter
(B) operator, promoter and repressor
(C) origin of replication, promoter and terminator
(D) promoter, structural gene and terminator
48.
A transcription unit in DNA is defined primarily by three regions,namely
(A) exon, intron and promoter
(B) operator, promoter and repressor
(C) origin of replication, promoter and terminator
(D) promoter, structural gene and terminator
49.
In the structural gene of a transcription unit, the strand that acts asthe template has the polarity
(A) 5′ → 3′ and the same sequence as RNA
(B) 3′ → 5′, since RNA polymerase catalyses polymerisation only in
the 5′ → 3′ direction
(C) 3′ → 5′ and is displaced during transcription
(D) 5′ → 3′ and carries the promoter
50.
In the structural gene of a transcription unit, the strand that acts asthe template has the polarity
(A) 5′ → 3′ and the same sequence as RNA
(B) 3′ → 5′, since RNA polymerase catalyses polymerisation only in
the 5′ → 3′ direction
(C) 3′ → 5′ and is displaced during transcription
(D) 5′ → 3′ and carries the promoter
51.
With reference to the coding strand, the promoter is locatedtowards the
(A) 3′-end of the structural gene, and it provides the binding site
for DNA ligase
(B) 5′-end (upstream) of the structural gene, and it provides the
binding site for RNA polymerase
(C) 3′-end of the structural gene, and it ends transcription
(D) 5′-end of the structural gene, and it binds the release factor
52.
With reference to the coding strand, the promoter is locatedtowards the
(A) 3′-end of the structural gene, and it provides the binding site
for DNA ligase
(B) 5′-end (upstream) of the structural gene, and it provides the
binding site for RNA polymerase
(C) 3′-end of the structural gene, and it ends transcription
(D) 5′-end of the structural gene, and it binds the release factor
53.
If the sequence of the coding strand in a transcription unit is 5′ATGCATGCATGCATGCATGCATGCATGC-3′, the sequence of themRNA transcribed from it is
(A) 5′-AUGCAUGCAUGCAUGCAUGCAUGCAUGC-3′
(B) 5′-UACGUACGUACGUACGUACGUACGUACG-3′
(C) 3′-AUGCAUGCAUGCAUGCAUGCAUGCAUGC-5′
(D) 5′-ATGCATGCATGCATGCATGCATGCATGC-3’
54.
If the sequence of the coding strand in a transcription unit is 5′ATGCATGCATGCATGCATGCATGCATGC-3′, the sequence of themRNA transcribed from it is
(A) 5′-AUGCAUGCAUGCAUGCAUGCAUGCAUGC-3′
(B) 5′-UACGUACGUACGUACGUACGUACGUACG-3′
(C) 3′-AUGCAUGCAUGCAUGCAUGCAUGCAUGC-5′
(D) 5′-ATGCATGCATGCATGCATGCATGCATGC-3’
55.
A cistron is a segment of DNA coding for a polypeptide. Thestructural gene in a transcription unit is
(A) polycistronic mostly in eukaryotes and monocistronic mostly in
bacteria
(B) monocistronic in both bacteria and eukaryotes
(C) monocistronic mostly in eukaryotes and polycistronic mostly in
bacteria
(D) polycistronic in both bacteria and eukaryotes
56.
A cistron is a segment of DNA coding for a polypeptide. Thestructural gene in a transcription unit is
(A) polycistronic mostly in eukaryotes and monocistronic mostly in
bacteria
(B) monocistronic in both bacteria and eukaryotes
(C) monocistronic mostly in eukaryotes and polycistronic mostly in
bacteria
(D) polycistronic in both bacteria and eukaryotes
57.
Sequences that appear in the mature or processed RNA are called______, while the intervening sequences
removed from the primary transcript are called ______.
(A) introns; exons
(B) cistrons; operons
(C) exons; introns
(D) promoters; terminators
58.
Sequences that appear in the mature or processed RNA are called______, while the intervening sequences
removed from the primary transcript are called ______.
(A) introns; exons
(B) cistrons; operons
(C) exons; introns
(D) promoters; terminators
59.
In bacteria, transcription of mRNA, tRNA and rRNA is catalysed by(A) a single DNA-dependent RNA polymerase
(B) three different RNA polymerases, one for each RNA
(C) DNA polymerase III
(D) RNA polymerases I, II and III
60.
In bacteria, transcription of mRNA, tRNA and rRNA is catalysed by(A) a single DNA-dependent RNA polymerase
(B) three different RNA polymerases, one for each RNA
(C) DNA polymerase III
(D) RNA polymerases I, II and III
61.
In bacteria, the RNA polymerase associates transiently with ______to initiate and with ______ to terminate transcription.
(A) rho factor; sigma factor
(B) DNA ligase; rho factor
(C) release factor; sigma factor
(D) sigma factor; rho factor
62.
In bacteria, the RNA polymerase associates transiently with ______to initiate and with ______ to terminate transcription.
(A) rho factor; sigma factor
(B) DNA ligase; rho factor
(C) release factor; sigma factor
(D) sigma factor; rho factor
63.
In eukaryotic nuclei, RNA polymerase III is responsible for thetranscription of
(A) 28S, 18S and 5.8S rRNAs
(B) tRNA, 5srRNA and snRNAs
(C) hnRNA, the precursor of mRNA
(D) mRNA directly without any processing
64.
In eukaryotic nuclei, RNA polymerase III is responsible for thetranscription of
(A) 28S, 18S and 5.8S rRNAs
(B) tRNA, 5srRNA and snRNAs
(C) hnRNA, the precursor of mRNA
(D) mRNA directly without any processing
65.
The cell-free system for protein synthesis that helped in decipheringthe genetic code was developed by
(A) Har Gobind Khorana
(B) Severo Ochoa
(C) Marshall Nirenberg
(D) George Gamow
66.
The cell-free system for protein synthesis that helped in decipheringthe genetic code was developed by
(A) Har Gobind Khorana
(B) Severo Ochoa
(C) Marshall Nirenberg
(D) George Gamow
67.
Which of the following codons does not code for any amino acid andhas no corresponding tRNA?
(A) UGG
(B) AUG
(C) UGA
(D) UGU
68.
Which of the following codons does not code for any amino acid andhas no corresponding tRNA?
(A) UGG
(B) AUG
(C) UGA
(D) UGU
69.
The nucleotide sequence of an mRNA cannot be predicted exactlyfrom the amino acid sequence Met-PhePhe-Phe-Phe-Phe-Phe,
because the genetic code is
(A) universal
(B) contiguous
(C) triplet
(D) degenerate
70.
The nucleotide sequence of an mRNA cannot be predicted exactlyfrom the amino acid sequence Met-PhePhe-Phe-Phe-Phe-Phe,
because the genetic code is
(A) universal
(B) contiguous
(C) triplet
(D) degenerate
71.
Charging (aminoacylation) of tRNA, the first phase of translation,requires
(A) ATP and the linking of the amino acid to its cognate tRNA
(B) GTP and the release factor
(C) NADPH and the ribosome
(D) DNA ligase and the small subunit
72.
Charging (aminoacylation) of tRNA, the first phase of translation,requires
(A) ATP and the linking of the amino acid to its cognate tRNA
(B) GTP and the release factor
(C) NADPH and the ribosome
(D) DNA ligase and the small subunit
73.
In bacteria, the enzyme (ribozyme) that catalyses peptide bondformation during translation is
(A) a protease in the small subunit
(B) DNA polymerase
(C) 23S rRNA of the large subunit
(D) 16S rRNA of the small subunit
74.
In bacteria, the enzyme (ribozyme) that catalyses peptide bondformation during translation is
(A) a protease in the small subunit
(B) DNA polymerase
(C) 23S rRNA of the large subunit
(D) 16S rRNA of the small subunit
75.
Untranslated regions (UTRs) of an mRNA are present(A) only at the 3′-end, after the stop codon
(B) only at the 5′-end, before the start codon
(C) at both the 5′-end (before the start codon) and the 3′-end (after the
stop codon)
(D) only within the translational unit between AUG and the stop codon
76.
Untranslated regions (UTRs) of an mRNA are present(A) only at the 3′-end, after the stop codon
(B) only at the 5′-end, before the start codon
(C) at both the 5′-end (before the start codon) and the 3′-end (after the
stop codon)
(D) only within the translational unit between AUG and the stop codon
77.
During initiation of translation, the start codon AUG is recognised onlyby the ______, and translation is terminated when a ______ binds to
the stop codon.
(A) initiator tRNA; release factor
(B) sigma factor; rho factor
(C) release factor; initiator tRNA
(D) charged tRNA of Phe; ribozyme
78.
During initiation of translation, the start codon AUG is recognised onlyby the ______, and translation is terminated when a ______ binds to
the stop codon.
(A) initiator tRNA; release factor
(B) sigma factor; rho factor
(C) release factor; initiator tRNA
(D) charged tRNA of Phe; ribozyme
79.
The operator region of an operon is generally(A) adjacent to the terminator and binds the release factor
(B) adjacent to the promoter and binds a repressor protein
(C) within the structural gene and binds the ribosome
(D) an inducer-binding site on the repressor gene
80.
The operator region of an operon is generally(A) adjacent to the terminator and binds the release factor
(B) adjacent to the promoter and binds a repressor protein
(C) within the structural gene and binds the ribosome
(D) an inducer-binding site on the repressor gene
81.
In the lac operon, the genes z, y and a code respectively for(A) permease, beta-galactosidase and transacetylase
(B) repressor, permease and beta-galactosidase
(C) transacetylase, permease and beta-galactosidase
(D) beta-galactosidase, permease and transacetylase
82.
In the lac operon, the genes z, y and a code respectively for(A) permease, beta-galactosidase and transacetylase
(B) repressor, permease and beta-galactosidase
(C) transacetylase, permease and beta-galactosidase
(D) beta-galactosidase, permease and transacetylase
83.
The term i in the i gene of the lac operon is derived from the word______ and the gene codes for the ______.
(A) inhibitor; repressor
(B) inducer; permease
(C) initiator; beta-galactosidase
(D) inhibitor; transacetylase
84.
The term i in the i gene of the lac operon is derived from the word______ and the gene codes for the ______.
(A) inhibitor; repressor
(B) inducer; permease
(C) initiator; beta-galactosidase
(D) inhibitor; transacetylase
85.
One approach of HGP identified all the genes expressed as RNA,called ______, while the other sequenced the whole genome and
later assigned functions to regions, called ______.
(A) SNPs; microsatellites
(B) Expressed Sequence Tags; Sequence Annotation
(C) Sequence Annotation; Expressed Sequence Tags
(D) BAC; YAC
86.
One approach of HGP identified all the genes expressed as RNA,called ______, while the other sequenced the whole genome and
later assigned functions to regions, called ______.
(A) SNPs; microsatellites
(B) Expressed Sequence Tags; Sequence Annotation
(C) Sequence Annotation; Expressed Sequence Tags
(D) BAC; YAC
87.
For sequencing in HGP, DNA fragments were cloned inbacteria and yeast using the vectors
(A) pBR322 and plasmids
(B) BAC and YAC
(C) cosmids and phagemids
(D) Ti plasmid and retrovirus
88.
For sequencing in HGP, DNA fragments were cloned inbacteria and yeast using the vectors
(A) pBR322 and plasmids
(B) BAC and YAC
(C) cosmids and phagemids
(D) Ti plasmid and retrovirus
89.
According to the salient features of the human genome, the largestknown human gene is ______ with 2.4 million bases, and the
chromosome with the fewest genes is
(A) insulin; chromosome 21
(B) dystrophin; chromosome 1
(C) beta globin; chromosome Y
(D) dystrophin; chromosome Y
90.
According to the salient features of the human genome, the largestknown human gene is ______ with 2.4 million bases, and the
chromosome with the fewest genes is
(A) insulin; chromosome 21
(B) dystrophin; chromosome 1
(C) beta globin; chromosome Y
(D) dystrophin; chromosome Y
91.
Single-base DNA differences occurring at about 1.4 million locations inthe human genome are known as
(A) SNPs
(B) VNTRs
(C) ESTs
(D) microsatellites
92.
Single-base DNA differences occurring at about 1.4 million locations inthe human genome are known as
(A) SNPs
(B) VNTRs - VNTRs are minisatellite tandem repeats used as Southern
blot probes
(C) ESTs - ESTs (Expressed Sequence Tags) are genes expressed as
RNA in HGP, not single nucleotide polymorphisms
(D) microsatellites - microsatellites are short repetitive DNA stretches
93.
The DNA fingerprint of an individual differs from that of every otherindividual in a population, except in the case of
(A) siblings
(B) cousins
(C) parent and child
(D) monozygotic (identical) twins
94.
The DNA fingerprint of an individual differs from that of every otherindividual in a population, except in the case of
(A) siblings
(B) cousins
(C) parent and child
(D) monozygotic (identical) twins
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