RIBONUCLEIC ACID (RNA)
P. HARITHA
DL BOTANY
TTWRDC M
SANGAREDDY
• Most prokaryotic and eukaryotic cells contain, another
important nucleic acid, the Ribonucleic acid(RNA)
besides DNA.
• Some viruses , however contain no DNA but only RNA.
• In them, RNA is the sole genetic material, and carries the
responsibilities of DNA.
• Such RNA is called Genetic RNA. E.g. TMV.
• Turnip yellow mosaic viruses, wound tumour viruses,
influenza viruses, polio viruses, etc.
• Further, in cells in which the genetic substance
is DNA, there occur another kind of molecules,
which are called Non-Genetic RNAs.
• Those RNAs depend on DNA for their synthesis and
are ultimately translated into the linear sequence of
amino acids in a polypeptide chain (protein
synthesis).
(A) Occurrence:
• Non-genetic RNA is generally found in the cytoplasm
and the nucleolus.
• In the cytoplasm, it is found freely but also found
associated with ribosomes.
• RNA is also found in mitochondria and chloroplast.
(B) Structure of RNA:
• RNA is an unbranched polynucleotide chain.
• It is formed by phosphodiester bonds between
ribonucleotides in 3’5’ direction.
• The number of ribonucleotides in RNA range form as few
as 75 to many thousands.
• RNA nucleotides have ribose sugar(in place of
deoxyribose in DNA), which participates in the formation
of sugar-phosphate back bone of RNA.
• The nitrogen bases are- adenine(A), guanine(G),
Cytosine(C) and Uracil(U).
• Uracil differs for thymine(T), of DNA in lacking a
methyl group(-CH3) at 5’C position
• These nitrogen bases do not show complementarity,
hence there is no 1:1 ratio between purines and
pyrimidines.
• .
(C) Types of RNA:
• Three types of non-genetic RNA molecules are found in
all prokaryotic and eukaryotic cells.
• Their synthesis is always dependent on DNA template.
• They are (i) Messenger RNA, (ii) Ribosomal RNA and
• (iii) Transfer RNA.
(i) Messenger RNA(m RNA):
• Messenger RNA carries genetic information from
chromosomal DNA to ribosome for protein synthesis, so
it functions as a messenger.
• Therefore, Jacob and Monod in 1961 named this RNA
as mRNA.
• It is 5% to 10% of the total quantity of RNA present in
the cytoplasm.
• The molecular weight of an average sized m-RNA is
5x106 daltons.
• m-RNA is formed as a complementary strand from
one of the two strands of DNA(Transcription).
• So the sequence of bases of each m-RNA is
complementary to antisense strand of DNA.
• The only difference is that in place of thymine, uracil is
present.
• It immediately diffuses into the cytoplasm, where protein
synthesis takes place.
• In prokaryotes, m-RNA is metabolically unstable with a
half-life time from a few seconds to about 2 minutes.
• Hence, transcription and translation proceed
simultaneously.
• But in eukaryotes, it is relatively stable with a half-life
ranging from a few hours to one day.
• Generally, a single prokaryotic mRNA molecule codes for
more than one polypeptide.
• Such an mRNA is known as polycistronic m-RNA.
• On the otherhand, all eukaryotic m-RNAs are
monocistronic i.e; code for a protein specified by a single
cistron.
Both eukaryotic and prokaryotic mRNAs have the
following features.
(1) A 5’ leader sequence, that is not translated.
(2) A coding region, which begins with about 1500
nucleotides, and this region translates protein.
(3) Non-coding region at the 3’ end.
• Both types of m RNA molecules are synthesized with
triphosphate group at the 5’ end, so there is no basic
difference between the two.
1. Prokaryotic m RNAs:
• In prokaryotes, different genes concerned with the same
trait are often found clustered together in a group known
as the Operon.
• All the genes present in an operon are transcribed into a
single mRNA molecule.
• These mRNA are polycistronic and carries the codes for
several adjacent DNA cistrons(genes).
• These mRNAs have no specified significance at the
5’ end(i.e., cap is absent).
• Hence, ribosomes can bind at many sites in the
interior of an m-RNA, each resulting in the synthesis
of different protein.
(2) Eukaryotic mRNAs:
• All eukaryotic mRNA molecules show the following
special structural features:
(a) Cap:
• A cap is found at the 5’ end of the mRNA in which
methylated guanine is present.
• This gives protection from the action of exonucleases
present in the cytoplasm.
(b) Non-Coding Region(NCR):
• Immediately after the cap, a region of 10 to 100 nucleotides
is present.
• In this region A and U are found in excess and does not
translate into protein.
• This sequence of nucleotides is called leader sequence.
(c) Initiation codon:
• In both prokaryotes and eukaryotes, primary codon AUG is
found.
(d) Coding region(CR):
• This region consists of about 1500 nucleotides, and this
region translates protein.
(e) Termination region(CR):
• The coding region ends with a termination codon.
• The termination codons in eukaryotic cell are UAA, UAG
and UGA.
(f) Poly-A sequence:
• At the 3’ end of mRNA, poly adenylate or Poly-
A(AAAA……A) sequence is found.
• Poly A sequence is added after transcription.
(ii) Ribosomal RNA(r-RNA):
Ribosomal RNA(or rRNA) or insoluble RNA(i-RNA) constitutes
the largest part(upto 80%) of the total cellular RNA.
It is primarily found in ribosomes.
It consists of a single strand of nucleotides, which is folded at
several places to form pseudohelices, where the bases show
complementary base pairing.
The r-RNA contains G-C content more than 50%.
• r-RNA molecules remain stable atleast upto two
generations.
• Ribosomes of prokaryotic cells are of 70s type and are
composed of 60% r-RNA and 40% proteins.
• They dissociate into a smaller 30S subunit and a larger
50S subunit.
• The 30S subunit has a single 16S r-RNA molecule, which
is associated with 21 different types of ‘S’ proteins.
• The larger subunit has a 23S rRNA and 5S r-RNA molecule
complexed with 31 different ‘L’ proteins.
• The cytoplasmic ribosomes of eukaryotes are the 80S size,
and contain 40%r-RNA and 60%protein.
• They consists of a 40S and 60S subunits.
• The 40S subunit has one molecule each of 28S, 58S and 5S
r-RNA and 49 different proteins.
(iii) Transfer RNA(t-RNA):
• Transfer RNA molecules are also called as soluble RNA or
adaptor RNA.
• T-RNA constitutes about 10-15% of the total weight of RNA
of the cell.
• It is the smallest form and is composed of 75-95
nucleotides and has a molecular weight of about 25,000.
• T-RNA molecules have a large number of unusual bases
viz., Dihydrouridine(DHU), Pesudouridine(), Inosine(I),
methylated bases and thymine(T).
• The unusual bases are produced after transcription by
modification of usual bases A, T, C, and G.
• Further, t-RNA molecules show considerable helical
structure, and more than 50% of the bases in t-RNA are
paired.
• The base sequence of alanine-t-RNA of yeast was the
first to be determined by Holley and co workers in 1964
• For this, he was awarded Nobel prize in 1968.
• The existence of t-RNA was demonstrated by Hoagland
and co workers in 1957.
• Holley(1965) proposed a clover leaf model for t-RNA
molecules to account for its structural and functional
properties.
• According to this model, a single polynucleotide chain of
t-RNA molecule is folded back on itself, by which the 3’-
end and 5’ end come together.
• In this way three major arms are formed.
• Each arm contains one stem and one loop.
• In the loop, unpaired bases are present.
• A typical clover-leaf model of t-RNA shows the following
structural peculiarities.
(i) All t-RNA molecules contain the same terminal
sequence of 5’-CCA-3’ bases at 3-end. The last residue,
adenine(A), is the amino acid attachment site.
(ii) The TC or thymine arm is located near the 3’-end and
has 7 unpaired bases. The TC arm is involved in the
binding of t-RNA molecules to the ribosomes.
(iii) The DHU or dihydrouridine loop is made up of 8-12
unpaired bases. It contain a site for the recognition of
the amino acyl synthetase enzyme.
(iv) The anticodon arm contains one nucleotide triplet which
is different in all t-RNA molecules. This is the codon
recognition site or anticodon and it is complementary to
the corresponding triplet codon of mRNA.
(v) Some t RNA with long chains may form a short, extra
arm.
• The clover-leaf model represents the secondary structure of
all the tRNA molecules.
• All t-RNA acquire an L-shaped tertiary structure, which is
critical for their function.
• In this configuration, the arms of DHU and anticodon arms
straighten to form one arm of the ‘L’.
• The TC arm and acceptor arms also straighten and twist to
form the other arm of ‘L’ in such a way that the TC loop lies
close to the D loop.
• Thus, the anticodon loop becomes located at the tip of one
arm of ‘L’, while the amino acid acceptor region is present at
the tip of the other arm.
• Both Clover-leaf and L-shaped configuration are
stabilized by H bonds.
• Transfer RNAs help in bringing the aminoacid to the
ribosomes and play a key role in protein synthesis.
• Since there are only 20 amino acids and around 32
different kinds of t-RNAs, some amino acids are carried
by more than one type of t- RNA.
THANK YOU

RNA.- a short view into sturcture and function of RNA

  • 1.
    RIBONUCLEIC ACID (RNA) P.HARITHA DL BOTANY TTWRDC M SANGAREDDY
  • 3.
    • Most prokaryoticand eukaryotic cells contain, another important nucleic acid, the Ribonucleic acid(RNA) besides DNA. • Some viruses , however contain no DNA but only RNA. • In them, RNA is the sole genetic material, and carries the responsibilities of DNA. • Such RNA is called Genetic RNA. E.g. TMV. • Turnip yellow mosaic viruses, wound tumour viruses, influenza viruses, polio viruses, etc.
  • 5.
    • Further, incells in which the genetic substance is DNA, there occur another kind of molecules, which are called Non-Genetic RNAs. • Those RNAs depend on DNA for their synthesis and are ultimately translated into the linear sequence of amino acids in a polypeptide chain (protein synthesis).
  • 6.
    (A) Occurrence: • Non-geneticRNA is generally found in the cytoplasm and the nucleolus. • In the cytoplasm, it is found freely but also found associated with ribosomes. • RNA is also found in mitochondria and chloroplast.
  • 7.
    (B) Structure ofRNA: • RNA is an unbranched polynucleotide chain. • It is formed by phosphodiester bonds between ribonucleotides in 3’5’ direction. • The number of ribonucleotides in RNA range form as few as 75 to many thousands. • RNA nucleotides have ribose sugar(in place of deoxyribose in DNA), which participates in the formation of sugar-phosphate back bone of RNA.
  • 8.
    • The nitrogenbases are- adenine(A), guanine(G), Cytosine(C) and Uracil(U). • Uracil differs for thymine(T), of DNA in lacking a methyl group(-CH3) at 5’C position • These nitrogen bases do not show complementarity, hence there is no 1:1 ratio between purines and pyrimidines. • .
  • 10.
    (C) Types ofRNA: • Three types of non-genetic RNA molecules are found in all prokaryotic and eukaryotic cells. • Their synthesis is always dependent on DNA template. • They are (i) Messenger RNA, (ii) Ribosomal RNA and • (iii) Transfer RNA.
  • 12.
    (i) Messenger RNA(mRNA): • Messenger RNA carries genetic information from chromosomal DNA to ribosome for protein synthesis, so it functions as a messenger. • Therefore, Jacob and Monod in 1961 named this RNA as mRNA. • It is 5% to 10% of the total quantity of RNA present in the cytoplasm.
  • 13.
    • The molecularweight of an average sized m-RNA is 5x106 daltons. • m-RNA is formed as a complementary strand from one of the two strands of DNA(Transcription). • So the sequence of bases of each m-RNA is complementary to antisense strand of DNA. • The only difference is that in place of thymine, uracil is present.
  • 15.
    • It immediatelydiffuses into the cytoplasm, where protein synthesis takes place. • In prokaryotes, m-RNA is metabolically unstable with a half-life time from a few seconds to about 2 minutes. • Hence, transcription and translation proceed simultaneously. • But in eukaryotes, it is relatively stable with a half-life ranging from a few hours to one day.
  • 16.
    • Generally, asingle prokaryotic mRNA molecule codes for more than one polypeptide. • Such an mRNA is known as polycistronic m-RNA. • On the otherhand, all eukaryotic m-RNAs are monocistronic i.e; code for a protein specified by a single cistron.
  • 17.
    Both eukaryotic andprokaryotic mRNAs have the following features. (1) A 5’ leader sequence, that is not translated. (2) A coding region, which begins with about 1500 nucleotides, and this region translates protein. (3) Non-coding region at the 3’ end.
  • 18.
    • Both typesof m RNA molecules are synthesized with triphosphate group at the 5’ end, so there is no basic difference between the two. 1. Prokaryotic m RNAs: • In prokaryotes, different genes concerned with the same trait are often found clustered together in a group known as the Operon. • All the genes present in an operon are transcribed into a single mRNA molecule. • These mRNA are polycistronic and carries the codes for several adjacent DNA cistrons(genes).
  • 19.
    • These mRNAshave no specified significance at the 5’ end(i.e., cap is absent). • Hence, ribosomes can bind at many sites in the interior of an m-RNA, each resulting in the synthesis of different protein.
  • 20.
    (2) Eukaryotic mRNAs: •All eukaryotic mRNA molecules show the following special structural features: (a) Cap: • A cap is found at the 5’ end of the mRNA in which methylated guanine is present. • This gives protection from the action of exonucleases present in the cytoplasm.
  • 21.
    (b) Non-Coding Region(NCR): •Immediately after the cap, a region of 10 to 100 nucleotides is present. • In this region A and U are found in excess and does not translate into protein. • This sequence of nucleotides is called leader sequence. (c) Initiation codon: • In both prokaryotes and eukaryotes, primary codon AUG is found. (d) Coding region(CR): • This region consists of about 1500 nucleotides, and this region translates protein.
  • 23.
    (e) Termination region(CR): •The coding region ends with a termination codon. • The termination codons in eukaryotic cell are UAA, UAG and UGA. (f) Poly-A sequence: • At the 3’ end of mRNA, poly adenylate or Poly- A(AAAA……A) sequence is found. • Poly A sequence is added after transcription.
  • 24.
    (ii) Ribosomal RNA(r-RNA): RibosomalRNA(or rRNA) or insoluble RNA(i-RNA) constitutes the largest part(upto 80%) of the total cellular RNA. It is primarily found in ribosomes. It consists of a single strand of nucleotides, which is folded at several places to form pseudohelices, where the bases show complementary base pairing. The r-RNA contains G-C content more than 50%.
  • 25.
    • r-RNA moleculesremain stable atleast upto two generations. • Ribosomes of prokaryotic cells are of 70s type and are composed of 60% r-RNA and 40% proteins. • They dissociate into a smaller 30S subunit and a larger 50S subunit. • The 30S subunit has a single 16S r-RNA molecule, which is associated with 21 different types of ‘S’ proteins.
  • 27.
    • The largersubunit has a 23S rRNA and 5S r-RNA molecule complexed with 31 different ‘L’ proteins. • The cytoplasmic ribosomes of eukaryotes are the 80S size, and contain 40%r-RNA and 60%protein. • They consists of a 40S and 60S subunits. • The 40S subunit has one molecule each of 28S, 58S and 5S r-RNA and 49 different proteins. (iii) Transfer RNA(t-RNA): • Transfer RNA molecules are also called as soluble RNA or adaptor RNA. • T-RNA constitutes about 10-15% of the total weight of RNA of the cell.
  • 30.
    • It isthe smallest form and is composed of 75-95 nucleotides and has a molecular weight of about 25,000. • T-RNA molecules have a large number of unusual bases viz., Dihydrouridine(DHU), Pesudouridine(), Inosine(I), methylated bases and thymine(T). • The unusual bases are produced after transcription by modification of usual bases A, T, C, and G.
  • 31.
    • Further, t-RNAmolecules show considerable helical structure, and more than 50% of the bases in t-RNA are paired. • The base sequence of alanine-t-RNA of yeast was the first to be determined by Holley and co workers in 1964 • For this, he was awarded Nobel prize in 1968. • The existence of t-RNA was demonstrated by Hoagland and co workers in 1957.
  • 32.
    • Holley(1965) proposeda clover leaf model for t-RNA molecules to account for its structural and functional properties. • According to this model, a single polynucleotide chain of t-RNA molecule is folded back on itself, by which the 3’- end and 5’ end come together. • In this way three major arms are formed. • Each arm contains one stem and one loop. • In the loop, unpaired bases are present.
  • 33.
    • A typicalclover-leaf model of t-RNA shows the following structural peculiarities. (i) All t-RNA molecules contain the same terminal sequence of 5’-CCA-3’ bases at 3-end. The last residue, adenine(A), is the amino acid attachment site. (ii) The TC or thymine arm is located near the 3’-end and has 7 unpaired bases. The TC arm is involved in the binding of t-RNA molecules to the ribosomes. (iii) The DHU or dihydrouridine loop is made up of 8-12 unpaired bases. It contain a site for the recognition of the amino acyl synthetase enzyme.
  • 34.
    (iv) The anticodonarm contains one nucleotide triplet which is different in all t-RNA molecules. This is the codon recognition site or anticodon and it is complementary to the corresponding triplet codon of mRNA. (v) Some t RNA with long chains may form a short, extra arm.
  • 35.
    • The clover-leafmodel represents the secondary structure of all the tRNA molecules. • All t-RNA acquire an L-shaped tertiary structure, which is critical for their function. • In this configuration, the arms of DHU and anticodon arms straighten to form one arm of the ‘L’.
  • 36.
    • The TCarm and acceptor arms also straighten and twist to form the other arm of ‘L’ in such a way that the TC loop lies close to the D loop. • Thus, the anticodon loop becomes located at the tip of one arm of ‘L’, while the amino acid acceptor region is present at the tip of the other arm.
  • 37.
    • Both Clover-leafand L-shaped configuration are stabilized by H bonds. • Transfer RNAs help in bringing the aminoacid to the ribosomes and play a key role in protein synthesis. • Since there are only 20 amino acids and around 32 different kinds of t-RNAs, some amino acids are carried by more than one type of t- RNA.
  • 38.