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Assignment Submission 01 Introductory Molecular Biology BMB – 103 Submitted to Dr. Md. Golam Kabir Professor Department of Biochemistry & Molecular Biology University of Chittagong Submitted by Mohammad Mushtak Fuad ID: 20604039 (Group B) Session: 2019-2020 First Year Department of Biochemistry & Molecular Biology University of Chittagong Problem 01 i) Complementary DNA Complementary DNA (cDNA) is a DNA copy of a messenger RNA (mRNA) molecule producedby reverse transcriptase, a DNA polymerase that can use either DNA or RNA as a template. Complementary DNA (cDNA) is synthesized in the laboratory from messenger RNA. cDNA isnot genomic DNA, because the transcript of genomic RNA has been processed (i.e., it lackspromoters and introns). The enzyme reverse transcriptase is used to synthesizedouble-stranded DNA that is a complementary copy of the mRNA. ii) Antiparallel Antiparallel is a term applied to two molecules that are side by side but run in oppositedirections. The two strands of DNA are antiparallel. The head of one strand is always laid against the tail ofthe other strand of DNA. iii) Right-Handed Helix Helices can be either right-handed or left-handed. With the line of sight along the helix's axis, if a clockwise screwing motion moves the helix awayfrom the observer, then it is called a right-handed helix; if towards the observer, then it is aleft-handed helix. Handedness (or chirality) is a property of the helix, not of the perspective: a right-handed helixcannot be turned to look like a left-handed one unless it is viewed in a mirror, and vice versa. Most hardware screw threads are right-handed helices. The alpha helix in biology as well as the A and B forms of DNA are also right-handed helices. iv) Major grooves and Minor grooves Double-helical nucleic acid molecules contain two grooves, called the major groove and theminor groove. These grooves arise because the glycosidic bonds of a base pair are notdiametrically opposite each other. The minor groove contains the pyrimidine O-2 and the purineN-3 of the base pair, and the major groove is on the opposite side of the pair. The methyl groupof thymine also lies in the major groove. In B-DNA, the major groove is wider (12 versus 6 Å)and deeper (8.5 versus 7.5 Å) than the minor groove. Problem 02 Temperature of Melting: (tm value) The Temperature of Melting (Tm) is defined as the temperature at which 50% of double stranded DNA is changed to single-standard DNA. The higher the melting temperature the greater the guanine-cytosine (GC) content of the DNA. Formula: Tm = 2 °C(A + T) + 4 °C(G + C) = °C Tm Cot Value: (cot1/2) The product of Co (the original concentration of denatured DNA) and t (time in seconds), giving a useful index of DNA renaturation. Cot1/2 is the value when 50% renaturation has occurred which can be used to estimate the length of unique DNA in a sample. Tm value dependency: Tm is not a constant value. It is an index of the thermal stability of a nucleic acid, and is dependent on such conditions as the base sequence, base number, nucleic acid concentration, solvent conditions (salt composition, organic solvent composition, pH), mismatch(non-complementary base pairs), nucleic acid analog (artificial nucleic acid) structure, etc. Problem 04 Formula: Tm = 2 °C(A + T) + 4 °C(G + C) = °C Tm Example: Determine the melting temperature for the sequence: TGCTCA ACGAGT There are 1 A, 2 Ts, 1 G and 2 Cs, plug into the formula. 2°C (1+2) + 4°C (1+2) =2°C (3) + 4°C (3) =6°C + 12 °C = 18°C Problem 04 Different Types of DNA Conformations DNA, the genetic information carrier molecule of the cell, is a long polymer of nucleotides and can adopt different types of structural conformations. The various types of conformations that the DNA can adopt depend on different factors such as: 1. 2. 3. 4. 5. Hydration level Salt concentration DNA sequence Quantity and direction of super-coiling Presence of chemically modified bases 6. 7. Different types of metal ions and its concentrations Presence of polyamines in solution. The most common types of structural conformations of DNA are named as: (1). A-DNA (2). B-DNA (3). Z-DNA Among these three types, the most abundant type of DNA is B-DNA, commonly known as Watson-Crick Model of DNA double helix. The present post describes the structural features of A, B and Z forms of DNA in a comparative manner. We will also discuss the similarities and differences between A-DNA, BDNA and Z-DNA. 1). A-DNA A-DNA is a rare type of structural conformation that a DNA can adopt under dehydratingconditions. A-DNA is a double stranded helical structure almost similar to B-DNA but with ashorter and more compact structural organization. A-DNA was discovered by Rosalind Franklinand the credit for the naming of A-DNA and B-DNA was also accounted to her. Importantstructural features of A-DNA are given below: A-DNA is formed from B-DNA under dehydrating condition. A-DNA is much wider and flatter than B-DNA. Similar to B-DNA, the A-DNA is also a right handed helix. The helix diameter of A-DNA is 26 Å. The helix pitch (height of a turn) of A-DNA is 28.6 Å. A DNA is 20 to 25% shorter than B-DNA due to the smaller rise per turn. A-DNA contains 11.6 base pairs per turn. The distance between the adjacent base pairs is 2.9 Å. The helical twist per base pair in A-DNA is 31⁰. A-DNA has an axial hole at the centre (hollow central core). In A-DNA the base pairs are inclined to the helical axis. Individual base pairs in A-DNA are 20⁰ tilted with respect to the helical axis. A-DNA has narrow and deep major groves. The minor groves of A-DNA are wide and shallow. The de-oxyribose sugar pucker in A-DNA is C3’endo form The conformation of glycoside bond in A-DNA is in Antiform. (2). B-DNA The B-DNA is the most common and predominate type of structural conformation of DNA in the cells. The DNA prefers to occur in B form under the natural physiological conditions (pH and salt concentration) in the cell. The BDNA is better described as the Watson – Crick Model of DNA described for the first time by James Watson and Francis Crick. Important structural features of B-DNA are given below: Majority of the DNA in a cell is in B-DNA conformation. B-DNA is a right handed helix. In B-DNA, the bases occupy at the core whereas the sugar phosphate backbone occurs at the peripheral portion of the helix. In B-DNA only the edges of the base pairs are exposed to the solvent. Each base pair in B-DNA has the same width. The width of A – T and G – C in B-DNA is 10.85 Å. The helical diameter of B-DNA is 20 Å. Each turn on helix in B-DNA possess a helical height of 34 Å. Each turn in the B-DNA consists of 10 base pairs. The distance between adjacent base pairs in B-DNA is 3.4 Å. Each base pair will have a helical twist of 36⁰ (360/10). The plain of inter-strand hydrogen bonds are perpendicular to the helical axis. B-DNA has a solid central core. The major grove of B-DNA is wide and deep. The minor grove of B-DNA is narrow and deep. The sugar pucker in B-DNA is C2’ endow form. The glycosidic bond conformation in B-DNA is in antiform. 3). Z-DNA Z-DNA is a left-handed double helical conformation of DNA in which the double helix winds to the left in a zigzag pattern. The DNA strand with complementary nucleotides with alternating purines and pyrimidines (such as poly-d(GC).poly-d(GC) or poly-d(AC).poly-d(GT)) can form ZDNA conformation at high salt concentration. The existence of Z DNA was discovered by Andres Wang and Alexander Rich. Z-DNA is one of the biologically active forms of DNA found in vivo in the cells. The exact biological function of Z-DNA is not clear. The Z-DNA is usually located upstream of the start site of a gene and thus it may have some role in the regulation ofgene expression. Important structural features of B-DNA are given below: The Z-DNA is a left handed helical structure. The double helix winds in a zig-zag pattern. The helical diameter of Z-DNA is 18 Å. The total height of a helix turn is 44 Å. The nucleotide pairs in Z-DNA occur as nucleotide dimmers. Each helical turn of Z-DNA contains 12 nucleotides (6 dimers). The helical turn per base pair in Z-DNA is 9⁰ for pyrimidine – purine step and 51⁰ for purine –pyrimidine step. The distance between each nucleotide is 7.4 Å. Z-DNA possesses a more or less flat major grove. The minor grove in Z-DNA is narrow and deep. Z-DNA has a solid core at the centre. The sugar pucker is C2’ endo for pyrimidine and C3’endo for purines. The glycosidic bond conformation is anti- for pyrimidines and syn- for purines. Problem 05 Chargaff's rules state that DNA from any species of any organism should have a 1:1 stoichiometric ratio (base pair rule) of purine and pyrimidine bases (A+G=T+C) and, more specifically, that the amount of guanine should be equal to cytosine and the amount of adenine should be equal to thymine. This pattern is found in both strands of the DNA. Therefore, If I have 30% of Guanine content of a DNA sequence, A+G = T+C A+30= T+30 (Guanine should be equal to Cytosine; according to Chargaff’s rule) Now, here remains 40% of whole the Adenine & Thymine. Hence, if we apply Chargaff’s rule again this two components should be equal too. 40/2+30 = 40/2+30 20+30 = 20+30 Adenine has a 20% contribution conforming DNA sequence. The Genome Type is GC. Because G+C= 60%. Problem 06 H-DNA (Triplex DNA) Triple-stranded DNA (also known as H-DNA or TriplexDNA) is a DNA structure in which three oligonucleotides wind around each other and form a triple helix. In triplestranded DNA, the third strand binds to a B-form DNA (via Watson–Crick base-pairing) double helix by forming Hoogsteen base pairs or reversed Hoogsteen hydrogen bonds. Nucleic acid triple helices (triplexes) ◮ oligonucleotide complexes made of three strands ◮ a DNA duplex and an RNA strand (RNA:DNA-DNA) or ◮ a DNA duplex and a single DNA strand (DNA:DNA-DNA) ◮ interaction of nucleic acids without requiring unwinding ◮ third strand binds major groove with sequence specificity ◮ forming Hoogsteen or reverse Hoogsteen hydrogen bonds ◮ with the purine-rich strand of the duplex