Chapter 12: DNA
The first scientist to help figure out what genes are made of was Frederick Griffith
Griffith injected mice with four different samples of bacteria
Disease-causing bacteria that had been heat-killed did not kill the mice
Harmless bacteria did not kill the mice
But when the two strains were mixed together, the mice died
Griffith concluded that genetic information could be passed from one bacterial strain to another
This experiment led Griffith to discover transformation, a process in which one strain of bacteria is changed by a gene or genes from another strain of bacteria
A team led by Oswald Avery tried to find out what molecule causes transformation
Avery and other scientists discovered that DNA stores and passes genetic information from one generation of bacteria to the next
Other scientists tried to confirm Avery’s discovery
Alfred Hershey and Martha Chase used viruses (tiny, nonliving particles that can infect living cells) to study DNA
A bacteriophage is a kind of virus that infects bacteria by sticking to the surface of the cell and injecting its genetic information into it
Hershey and Chase used a bacteriophage that had a DNA core and a protein coat to find out which part of the virus—the protein coat or the DNA core—entered bacterial cells
Hershey and Chase’s experiment with bacteriophages confirmed Avery’s results, convincing many scientists that DNA was the genetic material found in genes
The DNA that makes up genes must be capable of storing, copying, and passing on the genetic information in a cell
The genetic material stores information needed by every living cell
Before a cell divides, its genetic information must be copied
When a cell divides, each daughter cell must receive a complete copy of the genetic information
DNA is a nucleic acid made up of nucleotides joined into long strands or chains by covalent bonds
Nucleic acids are long molecules found in cell nuclei
Nucleotides are the building blocks of nucleic acids and are made up of three basic parts: a 5-carbon sugar called deoxyribose, a phosphate group, and a nitrogenous base
Nitrogenous bases are bases that have nitrogen in them
DNA has four kinds of nitrogenous bases: adenine, guanine, cytosine, and thymine
The nucleotides in a strand of DNA are joined by covalent bonds formed between the sugar of one nucleotide and the phosphate group of the next
The next step was to figure out how those long chains of nucleotides are arranged
Erwin Chargaff and Rosalind Franklin both helped solve the puzzle of the structure of DNA
Rosalind Franklin used a technique called X-ray diffraction to get information about the structure of the DNA molecule
Her X-ray pictures showed that the strands in DNA are twisted around each other in a shape known as a helix
She also showed that DNA is made of two strands
The clues in Franklin’s X-ray pattern allowed Watson and Crick to build a model that explained the specific structure and properties of DNA
Watson and Crick determined that DNA has the structure of a double helix that looks like a twisted ladder
The double-helix model explains Chargaff ’s rule of base pairing and how the two strands of DNA are held together
The two strands of DNA run in opposite directions, or, “antiparallel”
Because of this arrangement, the nitrogenous bases on both strands meet at the center of the molecule, allowing each strand of the double helix to carry a sequence of nucleotides
Watson and Crick discovered that hydrogen bonds could form between certain nitrogenous bases
Though hydrogen bonds are fairly weak forces, they have just enough force to hold the two strands of DNA together
These bonds would form only between certain base pairs: adenine paired with thymine, and guanine paired with cytosine
This nearly perfect fit between A–T and G–C nucleotides is known as base pairing
Watson and Crick realized that each strand of the double helix has all the information needed to make the other strand
Because each strand can be used to make the other strand, the strands are said to be complementary
Replication is the process of copying DNA prior to cell division; it makes sure that each daughter cell has the same complete set of DNA molecules
During DNA replication, the DNA molecule makes two new complementary strands, with each strand of the double helix serves as a template for the new strand
The two strands of the double helix separate, making two replication forks
As each new strand forms, new bases are added following the rules of base pairing
The end result is two DNA molecules, each identical to the other and to the original DNA molecule
DNA replication is carried out by special proteins called enzymes that pull apart a molecule of DNA by breaking the hydrogen bonds between base pairs and then unwinding the two strands
The principal enzyme involved in DNA replication is DNA polymerase
DNA polymerase joins individual nucleotides to make a new strand of DNA
DNA polymerase produces the sugar-phosphate bonds that join nucleotides together to form the new strands
DNA polymerase checks each new DNA strand so that each molecule is a close copy of the original
The telomere is the end part of the chromosome, a region in which DNA is difficult to replicate
Cells use a special enzyme called telomerase that makes it less likely that genes will be damaged or lost during replication of rapidly dividing cells
In most prokaryotic cells, replication starts from a single point, and it continues in two directions until the whole chromosome is copied
In eukaryotic cells, replication may begin in hundreds of places on the DNA molecule
Replication then occurs in both directions until each chromosome is completely copied
The first scientist to help figure out what genes are made of was Frederick Griffith
Griffith injected mice with four different samples of bacteria
Disease-causing bacteria that had been heat-killed did not kill the mice
Harmless bacteria did not kill the mice
But when the two strains were mixed together, the mice died
Griffith concluded that genetic information could be passed from one bacterial strain to another
This experiment led Griffith to discover transformation, a process in which one strain of bacteria is changed by a gene or genes from another strain of bacteria
A team led by Oswald Avery tried to find out what molecule causes transformation
Avery and other scientists discovered that DNA stores and passes genetic information from one generation of bacteria to the next
Other scientists tried to confirm Avery’s discovery
Alfred Hershey and Martha Chase used viruses (tiny, nonliving particles that can infect living cells) to study DNA
A bacteriophage is a kind of virus that infects bacteria by sticking to the surface of the cell and injecting its genetic information into it
Hershey and Chase used a bacteriophage that had a DNA core and a protein coat to find out which part of the virus—the protein coat or the DNA core—entered bacterial cells
Hershey and Chase’s experiment with bacteriophages confirmed Avery’s results, convincing many scientists that DNA was the genetic material found in genes
The DNA that makes up genes must be capable of storing, copying, and passing on the genetic information in a cell
The genetic material stores information needed by every living cell
Before a cell divides, its genetic information must be copied
When a cell divides, each daughter cell must receive a complete copy of the genetic information
DNA is a nucleic acid made up of nucleotides joined into long strands or chains by covalent bonds
Nucleic acids are long molecules found in cell nuclei
Nucleotides are the building blocks of nucleic acids and are made up of three basic parts: a 5-carbon sugar called deoxyribose, a phosphate group, and a nitrogenous base
Nitrogenous bases are bases that have nitrogen in them
DNA has four kinds of nitrogenous bases: adenine, guanine, cytosine, and thymine
The nucleotides in a strand of DNA are joined by covalent bonds formed between the sugar of one nucleotide and the phosphate group of the next
The next step was to figure out how those long chains of nucleotides are arranged
Erwin Chargaff and Rosalind Franklin both helped solve the puzzle of the structure of DNA
Rosalind Franklin used a technique called X-ray diffraction to get information about the structure of the DNA molecule
Her X-ray pictures showed that the strands in DNA are twisted around each other in a shape known as a helix
She also showed that DNA is made of two strands
The clues in Franklin’s X-ray pattern allowed Watson and Crick to build a model that explained the specific structure and properties of DNA
Watson and Crick determined that DNA has the structure of a double helix that looks like a twisted ladder
The double-helix model explains Chargaff ’s rule of base pairing and how the two strands of DNA are held together
The two strands of DNA run in opposite directions, or, “antiparallel”
Because of this arrangement, the nitrogenous bases on both strands meet at the center of the molecule, allowing each strand of the double helix to carry a sequence of nucleotides
Watson and Crick discovered that hydrogen bonds could form between certain nitrogenous bases
Though hydrogen bonds are fairly weak forces, they have just enough force to hold the two strands of DNA together
These bonds would form only between certain base pairs: adenine paired with thymine, and guanine paired with cytosine
This nearly perfect fit between A–T and G–C nucleotides is known as base pairing
Watson and Crick realized that each strand of the double helix has all the information needed to make the other strand
Because each strand can be used to make the other strand, the strands are said to be complementary
Replication is the process of copying DNA prior to cell division; it makes sure that each daughter cell has the same complete set of DNA molecules
During DNA replication, the DNA molecule makes two new complementary strands, with each strand of the double helix serves as a template for the new strand
The two strands of the double helix separate, making two replication forks
As each new strand forms, new bases are added following the rules of base pairing
The end result is two DNA molecules, each identical to the other and to the original DNA molecule
DNA replication is carried out by special proteins called enzymes that pull apart a molecule of DNA by breaking the hydrogen bonds between base pairs and then unwinding the two strands
The principal enzyme involved in DNA replication is DNA polymerase
DNA polymerase joins individual nucleotides to make a new strand of DNA
DNA polymerase produces the sugar-phosphate bonds that join nucleotides together to form the new strands
DNA polymerase checks each new DNA strand so that each molecule is a close copy of the original
The telomere is the end part of the chromosome, a region in which DNA is difficult to replicate
Cells use a special enzyme called telomerase that makes it less likely that genes will be damaged or lost during replication of rapidly dividing cells
In most prokaryotic cells, replication starts from a single point, and it continues in two directions until the whole chromosome is copied
In eukaryotic cells, replication may begin in hundreds of places on the DNA molecule
Replication then occurs in both directions until each chromosome is completely copied