Hey, everyone. So when we talk about DNA or RNA base pairing, we need to talk about the intermolecular force of hydrogen bonding. Now, hydrogen bonding between the bases provides or produces a stabilizing effect towards the overall integrity of the structure. Here we are going to say that individually, hydrogen bonds are relatively weak, but collectively they are strong. This is one of the landmark ideas when it comes to hydrogen bondings when we discuss DNA later on. It's just that there are so many hydrogen bonds that exist within DNA; overall together, they are strong. They hold the DNA molecule together. With this idea, we have what's called complementary base pairing. Basically, this discusses the bonding preferences between different bases. This base bonds or hydrogen bonds to this particular base. Here we're going to say the binding preferences of A with, when we talk about, T or U, and then when we talk about G with C. Here, we're going to say that these complementary base pairings have a set number of hydrogen bonds that they do with one another. So, we're going to say A with T or U, will make 2 hydrogen bonds and G with C makes 3 hydrogen bonds. Remember we talked about this stabilizing effect. A with T or A with U makes 2 hydrogen bonds, which helps with overall integrity when you collectively add them together. But G with C, you're making 3 hydrogen bonds here. That's even more stability involved. You'll tend to see that places within DNA where we see G with C forming 3 hydrogen bonds are areas of increased strength. Here, if we take a look, in this image, we have different nitrogenous bases. We're showing their bonding preferences as well as the number of hydrogen bonds they make with each other. A with T, they're making 2, G and C, they're making 3 hydrogen bonds. In DNA, we're going to say here that A pairs with T, but in RNA, remember, we have the nitrogenous base of uracil. Here, A pairs with U instead. And then with both of them, C will always pair up with G. So just remember, when it comes to DNA, it's A with T. When it comes to RNA, A does not bond with T, A bonds with U instead. Because in RNA, we substitute out Thymine for uracil. So just remember that distinction. When it comes to DNA or RNA, Cytosine will always hydrogen bond to Guanine.
- 1. Matter and Measurements4h 29m
- What is Chemistry?5m
- The Scientific Method9m
- Classification of Matter16m
- States of Matter8m
- Physical & Chemical Changes19m
- Chemical Properties8m
- Physical Properties5m
- Intensive vs. Extensive Properties13m
- Temperature (Simplified)9m
- Scientific Notation13m
- SI Units (Simplified)5m
- Metric Prefixes24m
- Significant Figures (Simplified)11m
- Significant Figures: Precision in Measurements7m
- Significant Figures: In Calculations19m
- Conversion Factors (Simplified)15m
- Dimensional Analysis22m
- Density12m
- Specific Gravity9m
- Density of Geometric Objects19m
- Density of Non-Geometric Objects9m
- 2. Atoms and the Periodic Table5h 23m
- The Atom (Simplified)9m
- Subatomic Particles (Simplified)12m
- Isotopes17m
- Ions (Simplified)22m
- Atomic Mass (Simplified)17m
- Atomic Mass (Conceptual)12m
- Periodic Table: Element Symbols6m
- Periodic Table: Classifications11m
- Periodic Table: Group Names8m
- Periodic Table: Representative Elements & Transition Metals7m
- Periodic Table: Elemental Forms (Simplified)6m
- Periodic Table: Phases (Simplified)8m
- Law of Definite Proportions9m
- Atomic Theory9m
- Rutherford Gold Foil Experiment9m
- Wavelength and Frequency (Simplified)5m
- Electromagnetic Spectrum (Simplified)11m
- Bohr Model (Simplified)9m
- Emission Spectrum (Simplified)3m
- Electronic Structure4m
- Electronic Structure: Shells5m
- Electronic Structure: Subshells4m
- Electronic Structure: Orbitals11m
- Electronic Structure: Electron Spin3m
- Electronic Structure: Number of Electrons4m
- The Electron Configuration (Simplified)22m
- Electron Arrangements5m
- The Electron Configuration: Condensed4m
- The Electron Configuration: Exceptions (Simplified)12m
- Ions and the Octet Rule9m
- Ions and the Octet Rule (Simplified)8m
- Valence Electrons of Elements (Simplified)5m
- Lewis Dot Symbols (Simplified)7m
- Periodic Trend: Metallic Character4m
- Periodic Trend: Atomic Radius (Simplified)7m
- 3. Ionic Compounds2h 18m
- Periodic Table: Main Group Element Charges12m
- Periodic Table: Transition Metal Charges6m
- Periodic Trend: Ionic Radius (Simplified)5m
- Periodic Trend: Ranking Ionic Radii8m
- Periodic Trend: Ionization Energy (Simplified)9m
- Periodic Trend: Electron Affinity (Simplified)8m
- Ionic Bonding6m
- Naming Monoatomic Cations6m
- Naming Monoatomic Anions5m
- Polyatomic Ions25m
- Naming Ionic Compounds11m
- Writing Formula Units of Ionic Compounds7m
- Naming Ionic Hydrates6m
- Naming Acids18m
- 4. Molecular Compounds2h 18m
- Covalent Bonds6m
- Naming Binary Molecular Compounds6m
- Molecular Models4m
- Bonding Preferences6m
- Lewis Dot Structures: Neutral Compounds (Simplified)8m
- Multiple Bonds4m
- Multiple Bonds (Simplified)6m
- Lewis Dot Structures: Multiple Bonds10m
- Lewis Dot Structures: Ions (Simplified)8m
- Lewis Dot Structures: Exceptions (Simplified)12m
- Resonance Structures (Simplified)5m
- Valence Shell Electron Pair Repulsion Theory (Simplified)4m
- Electron Geometry (Simplified)8m
- Molecular Geometry (Simplified)11m
- Bond Angles (Simplified)11m
- Dipole Moment (Simplified)15m
- Molecular Polarity (Simplified)7m
- 5. Classification & Balancing of Chemical Reactions3h 17m
- Chemical Reaction: Chemical Change5m
- Law of Conservation of Mass5m
- Balancing Chemical Equations (Simplified)13m
- Solubility Rules16m
- Molecular Equations18m
- Types of Chemical Reactions12m
- Complete Ionic Equations18m
- Calculate Oxidation Numbers15m
- Redox Reactions17m
- Spontaneous Redox Reactions8m
- Balancing Redox Reactions: Acidic Solutions17m
- Balancing Redox Reactions: Basic Solutions17m
- Balancing Redox Reactions (Simplified)13m
- Galvanic Cell (Simplified)16m
- 6. Chemical Reactions & Quantities2h 35m
- 7. Energy, Rate and Equilibrium3h 46m
- Nature of Energy6m
- First Law of Thermodynamics7m
- Endothermic & Exothermic Reactions7m
- Bond Energy14m
- Thermochemical Equations12m
- Heat Capacity19m
- Thermal Equilibrium (Simplified)8m
- Hess's Law23m
- Rate of Reaction11m
- Energy Diagrams12m
- Chemical Equilibrium7m
- The Equilibrium Constant14m
- Le Chatelier's Principle23m
- Solubility Product Constant (Ksp)17m
- Spontaneous Reaction10m
- Entropy (Simplified)9m
- Gibbs Free Energy (Simplified)18m
- 8. Gases, Liquids and Solids3h 25m
- Pressure Units6m
- Kinetic Molecular Theory14m
- The Ideal Gas Law18m
- The Ideal Gas Law Derivations13m
- The Ideal Gas Law Applications6m
- Chemistry Gas Laws16m
- Chemistry Gas Laws: Combined Gas Law12m
- Standard Temperature and Pressure14m
- Dalton's Law: Partial Pressure (Simplified)13m
- Gas Stoichiometry18m
- Intermolecular Forces (Simplified)19m
- Intermolecular Forces and Physical Properties11m
- Atomic, Ionic and Molecular Solids10m
- Heating and Cooling Curves30m
- 9. Solutions4h 10m
- Solutions6m
- Solubility and Intermolecular Forces18m
- Solutions: Mass Percent6m
- Percent Concentrations10m
- Molarity18m
- Osmolarity15m
- Parts per Million (ppm)13m
- Solubility: Temperature Effect8m
- Intro to Henry's Law4m
- Henry's Law Calculations12m
- Dilutions12m
- Solution Stoichiometry14m
- Electrolytes (Simplified)13m
- Equivalents11m
- Molality15m
- The Colligative Properties15m
- Boiling Point Elevation16m
- Freezing Point Depression9m
- Osmosis16m
- Osmotic Pressure9m
- 10. Acids and Bases3h 29m
- Acid-Base Introduction11m
- Arrhenius Acid and Base6m
- Bronsted Lowry Acid and Base18m
- Acid and Base Strength17m
- Ka and Kb12m
- The pH Scale19m
- Auto-Ionization9m
- pH of Strong Acids and Bases9m
- Acid-Base Equivalents14m
- Acid-Base Reactions7m
- Gas Evolution Equations (Simplified)6m
- Ionic Salts (Simplified)23m
- Buffers25m
- Henderson-Hasselbalch Equation16m
- Strong Acid Strong Base Titrations (Simplified)10m
- 11. Nuclear Chemistry56m
- BONUS: Lab Techniques and Procedures1h 38m
- BONUS: Mathematical Operations and Functions47m
- 12. Introduction to Organic Chemistry1h 34m
- 13. Alkenes, Alkynes, and Aromatic Compounds2h 12m
- 14. Compounds with Oxygen or Sulfur1h 6m
- 15. Aldehydes and Ketones1h 1m
- 16. Carboxylic Acids and Their Derivatives1h 11m
- 17. Amines38m
- 18. Amino Acids and Proteins1h 51m
- 19. Enzymes1h 37m
- 20. Carbohydrates1h 46m
- Intro to Carbohydrates4m
- Classification of Carbohydrates4m
- Fischer Projections4m
- Enantiomers vs Diastereomers8m
- D vs L Enantiomers8m
- Cyclic Hemiacetals8m
- Intro to Haworth Projections4m
- Cyclic Structures of Monosaccharides11m
- Mutarotation4m
- Reduction of Monosaccharides10m
- Oxidation of Monosaccharides7m
- Glycosidic Linkage14m
- Disaccharides7m
- Polysaccharides7m
- 21. The Generation of Biochemical Energy2h 8m
- 22. Carbohydrate Metabolism2h 22m
- 23. Lipids2h 26m
- Intro to Lipids6m
- Fatty Acids25m
- Physical Properties of Fatty Acids6m
- Waxes4m
- Triacylglycerols12m
- Triacylglycerol Reactions: Hydrogenation8m
- Triacylglycerol Reactions: Hydrolysis13m
- Triacylglycerol Reactions: Oxidation7m
- Glycerophospholipids15m
- Sphingomyelins13m
- Steroids15m
- Cell Membranes7m
- Membrane Transport10m
- 24. Lipid Metabolism1h 45m
- 25. Protein and Amino Acid Metabolism1h 37m
- 26. Nucleic Acids and Protein Synthesis2h 54m
- Intro to Nucleic Acids4m
- Nitrogenous Bases16m
- Nucleoside and Nucleotide Formation9m
- Naming Nucleosides and Nucleotides13m
- Phosphodiester Bond Formation7m
- Primary Structure of Nucleic Acids11m
- Base Pairing10m
- DNA Double Helix6m
- Intro to DNA Replication20m
- Steps of DNA Replication11m
- Types of RNA10m
- Overview of Protein Synthesis4m
- Transcription: mRNA Synthesis9m
- Processing of pre-mRNA5m
- The Genetic Code6m
- Introduction to Translation7m
- Translation: Protein Synthesis18m
Base Pairing - Online Tutor, Practice Problems & Exam Prep
DNA and RNA rely on hydrogen bonding for base pairing, which stabilizes their structures. Adenine (A) pairs with thymine (T) in DNA, forming 2 hydrogen bonds, while in RNA, A pairs with uracil (U). Guanine (G) pairs with cytosine (C) in both, creating 3 hydrogen bonds, enhancing stability. The collective strength of these hydrogen bonds is crucial for the integrity of nucleic acids, with G-C pairs indicating regions of increased strength. Understanding these interactions is essential for grasping genetic coding and molecular biology.
Base Pairing Concept 1
Video transcript
Base Pairing Example 1
Video transcript
Here in this example, it says write in the missing bases and hydrogen bonds from the given image. Now if we take a look at this image, we can see that we see U involved. So U stands for uracil. This will represent base pairing with RNA. Alright. So, let's just go over the missing nitrogenous bases first. So A, since this is RNA, would hydrogen bond to U. Here we have U, so this would be an A. Over here we have a C, so this will be a G. Here we have a G, so this will be a C. Then coming back, remember that cytosine and guanine, C and G, form 3 hydrogen bonds to each other. It's fine. We have hydrogen bonds with all of these, and then down here, A with U, they form 2 hydrogen bonds. So, this is what we'd say in terms of our missing nitrogenous bases as well as our missing hydrogen bonds.
Four species shown below give the percentages of A–T pairings vs G–C pairings. Based on only the information given, which species would have the most significant strength in their base interactions?
Drosophila melanogaster (fruit fly) (55% : 45%)
Zea mays (corn) (51% : 49%)
Neurospora crassa (fungus) (46% : 54%)
Escherichia coli (bacteria) (49% : 51%)
Base Pairing Concept 2
Video transcript
Now with DNA base pairs, we have Chargaff's rule. In the early 1950s, Erwin Chargaff made an important discovery related to double-stranded DNA. Chargaff's rule states that for each species, no matter what it is, the percentage of A and T bases are roughly equal, as are the percentage of G and C bases. Remember, with DNA, A and T will hydrogen bond to each other. So, if they're hydrogen bonding with each other, we want them to have the same number. We have x number of A, we'd have to have the same x number of T. If we take a look here at the scale, let's just imagine that in this given species, this represents all of our A nitrogenous bases and this would have to represent all our T nitrogenous bases. If they're going to hydrogen bond to each other, the numbers need to be equal, so the percentages are equal. In the same way, G and C, they're going to hydrogen bond to each other, so they need to have equal numbers of both. So, putting it on a scale, G and C would have to be equal to each other. And this is Chargaff's rule. Because these base pairings exist, you have to have equal numbers of these pairings. So, A and T would have to be equal in percentage. G and C would have to be equal in percentage. Collectively, they represent 100% of all the nitrogenous bases within a given species. Also, remember here, you can see that the number of A and T's are different from the numbers in G and C's. It's these two being equal to each other in amount or percentages and these being equal to each other in amount or percentages. Okay. So it doesn't mean that they are all equal to each other. Right. So we'll take a look at when it comes to mathematical questions when it's talking about Chargaff's rule, and how we can apply it to understanding the percentages of a given nitrogenous base within any given species. But just remember, fundamentally, A and T percentages have to equal each other. G and C percentages have to equal each other.
Base Pairing Example 2
Video transcript
Here in this example question, it says human DNA is comprised of approximately 20% of adenine (A). It asks approximately what percentage of the nucleotides in a human DNA sample will be guanine (G). So we're going to list A, T, and then we have G and C. These are our base pairings. We're going to say collectively, they represent 100% of all the nitrogenous bases within a given species, in this case, a human being. Remember that the percentages between A and T have to be the same. So if Adenine is 20%, that means Thymine has to be 20%. So this equals 20%. This equals 20%. So we have 40% from just these two.
If we subtract that from 100%, that means we have 60% remaining. The 60% remaining represents G and C bases. Again, they have to be equal to each other in percentages as well. So of the 60%, 30% would have to be G, and 30% would have to be C. Again, according to Chargaff's rule, their percentages have to be equal. If A is 20%, T has to be 20%. They roughly have to be the same percentage. And then if you subtract that from 100%, that'll tell you your percentage left for G and C. They themselves also have to be roughly equal to each other. So just divide this number by 2 you would see that each one will be 30%. If we look at our options, the answer would have to be A. A human's DNA sample of guanine would have to be 30%.
Cytosine (C) makes up 42% of the nucleotides in a sample of DNA from an organism. Approximately what percentage of the nucleotides in this sample will be thymine (T)?
8%
16%
21%
60%
Do you want more practice?
Here’s what students ask on this topic:
What is the significance of hydrogen bonding in DNA and RNA base pairing?
Hydrogen bonding is crucial for the stability and integrity of DNA and RNA structures. In DNA, adenine (A) pairs with thymine (T) via 2 hydrogen bonds, while guanine (G) pairs with cytosine (C) through 3 hydrogen bonds. In RNA, adenine pairs with uracil (U) instead of thymine. These hydrogen bonds, although individually weak, collectively provide significant strength to the nucleic acid structures. The G-C pairs, with their 3 hydrogen bonds, contribute to regions of increased stability. Understanding these interactions is essential for comprehending genetic coding and molecular biology.
How do adenine and thymine pair in DNA, and how does this differ in RNA?
In DNA, adenine (A) pairs with thymine (T) through 2 hydrogen bonds. This pairing is specific and contributes to the double-helix structure's stability. In RNA, however, adenine pairs with uracil (U) instead of thymine. This substitution occurs because RNA contains uracil in place of thymine. Despite this difference, the hydrogen bonding mechanism remains similar, with A-U pairs also forming 2 hydrogen bonds. This distinction is crucial for understanding the structural differences between DNA and RNA.
Why are G-C pairs more stable than A-T pairs in DNA?
Guanine (G) and cytosine (C) pairs are more stable than adenine (A) and thymine (T) pairs because G-C pairs form 3 hydrogen bonds, while A-T pairs form only 2. The additional hydrogen bond in G-C pairs provides extra stability to the DNA structure. This increased stability is particularly important in regions of the DNA that require higher structural integrity. The collective strength of these hydrogen bonds is essential for maintaining the overall stability and integrity of the DNA molecule.
What role do complementary base pairings play in the structure of DNA and RNA?
Complementary base pairings are fundamental to the structure and function of DNA and RNA. In DNA, adenine (A) pairs with thymine (T), and guanine (G) pairs with cytosine (C). In RNA, adenine pairs with uracil (U) instead of thymine. These specific pairings, facilitated by hydrogen bonds, ensure the accurate replication and transcription of genetic information. The complementary nature of these pairings allows for the double-helix structure in DNA and the proper folding and function of RNA molecules. Understanding these pairings is crucial for studying genetic coding and molecular biology.
How does the number of hydrogen bonds between base pairs affect the stability of DNA?
The number of hydrogen bonds between base pairs directly affects the stability of DNA. Adenine (A) pairs with thymine (T) through 2 hydrogen bonds, while guanine (G) pairs with cytosine (C) through 3 hydrogen bonds. The additional hydrogen bond in G-C pairs provides greater stability compared to A-T pairs. Regions of DNA with a higher proportion of G-C pairs are more stable and less prone to denaturation. This increased stability is crucial for maintaining the integrity of the genetic material, especially in regions that require higher structural strength.
Your GOB Chemistry tutor
- (a) DNA and RNA, like proteins, can be denatured to produce unfolded or uncoiled strands. Heating DNA to what ...
- a. What is meant by the term base pairing?
- What does it mean to speak of bases as being complementary?
- The DNA from sea urchins contains about 32% A and about 18% G. What percentages of T and C would you expect in...
- If a double-stranded DNA molecule is 22% G, what is the percentage of A, T, and C? Explain.
- Write the base sequence in a complementary DNA segment if each original segment has the following base sequenc...
- Write the base sequence in a complementary DNA segment if each original segment has the following base sequenc...
- If the DNA double helix in salmon contains 28% adenine, what is the percentage of thymine, guanine, and cytos...