2 - Chromosome Compaction
The Part 2 reading assignment is divided into two sections. The first section will discuss how very large DNA molecules are compacted to fit inside virus particles, prokaryotic cells, and eukaryotic cells. This process of packaging DNA inside cells is called chromosome compaction. Chromosome compaction is actually a significant problem for all organisms. For example, a virus called bacteriophage lambda can package a 17 micrometer (µm) long nucleic acid molecule into a virus particle less than 0.1 µm in diameter (~200 times compaction); the intestinal bacterium E. coli can package a chromosome 1.2 millimeters (mm) in length in a cell that is 0.002 mm long (~1000 times compaction). Human cells package into the nucleus a genome that is 200,000 times longer than the diameter of the nucleus!
The second section in Part 2 will explore the process of X chromosome inactivation (XCI). X chromosome inactivation involves compacting one of the two X chromosomes found in the cells of female mammals to produce a condensed structure called a Barr body. This compaction of the X chromosome effectively silences one copy of every X-linked gene in the cell.
A. Chromosome Compaction Strategies in Prokaryotes and Eukaryotes
Bacterial Chromosome Compaction
The bacterial chromosome must be compacted approximately 500–1000 times to fit into the nucleoid region within a bacterial cell. To compact the DNA about tenfold, the bacterial cell forms microdomains within the chromosome (see Figure 2.1). Each microdomain is a loop connected to a centralized core structure through DNA binding proteins. The E. coli chromosome forms 400 to 500 microdomains, each of which contains approximately 10,000 base pairs (bp) of DNA. Adjacent microdomains are further bundled together to create regions called macrodomains. Each macrodomain contains 80–100 microdomains. Microdomains and macrodomains are formed when the repetitive DNA sequences (see Part 1) within bacterial DNA bind to proteins called nucleoid-associated proteins (NAPs). Some examples of NAPs include histone-like nucleoid structuring (H-NS) proteins and structural maintenance of chromosomes (SMC) proteins.
To compact the bacterial DNA even further, microdomains are supercoiled (i.e., twists are introduced into the microdomains) to fit the DNA within the nucleoid region of the cell (see Figure 2.1). Topoisomerases (see below) are a group of enzymes that direct the supercoiling of E. coli DNA.
- What are the three levels of chromosome compaction in prokaryotic cells?
- How are microdomains formed?
- What are macrodomains?
- What is meant by supercoiling?
Suppose a piece of linear double-stranded DNA is connected to two supports, one on each end of the molecule. Also suppose that the bottom support is held firmly in place, while the other support is twisted in the left-handed or counterclockwise direction. Since DNA is naturally a right-handed helix (the two DNA strands interact to produce a helix that rotates clockwise), introducing counterclockwise twists produces underwinding of the DNA double helix.
Underwinding of the DNA double helix produces fewer turns in the helix. For example, a linear 50 base pair (bp) DNA molecule with five turns in the double helix (10 bp per turn) would have 12.5 bp per turn if it is underwound by one turn (50 bp/4 turns = 12.5 bp/turn) (see the left-hand side of Figure 2.2). This linear form of DNA with 12.5 bp per turn is an unstable structure that does not naturally occur in cells. Instead, the underwound DNA molecule produces a negative supercoil, an attempt by the DNA double helix to stabilize itself. This negative supercoil produces a kink in the DNA molecule that causes the distance between the ends of the DNA to decrease. Negative supercoils are observed within bacterial chromosomes and function to compact the bacterial DNA into the nucleoid.
Overwinding, twisting the DNA double helix in the right-hand direction, increases the number of turns in the helix. For example, a 50 bp DNA molecule with five turns in the double helix (10 bp per turn) would have 8.3 bp per turn if it is overwound by one turn (50 bp/6 turns = 8.3 bp/turn) (see the right-hand side of Figure 2.2). This linear form of DNA with 8.3 bp per turn is an unstable structure that does not naturally occur in cells. The DNA molecule attempts to stabilize itself by producing supercoiling. This time, the supercoils are called positive supercoils. A positive supercoil produces a kink in the DNA molecule that causes the distance between the ends of the DNA to decrease.
A DNA molecule that lacks supercoils, has a single negative supercoil, or has a single positive supercoil can be converted into each other easily using topoisomerase enzymes (see below). These DNA molecules have the same base pair sequence and only differ in the degree of supercoiling. As a result, these three DNA molecules are considered to be topoisomers of each other.
- What is meant by positive and negative supercoiling?
Bacteria prefer negative supercoiling to positive supercoiling. In fact, typical bacterial chromosomes contain approximately one negative supercoil per 400 base pairs. Negative supercoiling is preferred because negative supercoiling:
- Compacts the chromosomal DNA into the nucleoid of the cell.
- Promotes DNA strand separation. Separation of the DNA strands is required for DNA replication and transcription.
Note that positive supercoiling compacts the chromosomal DNA to the same extent as negative supercoiling; however, positive supercoiling is inhibitory to DNA replication and transcription.
- What impact does supercoiling have on chromosome structure and function?
- Which one do you think would enhance transcription and DNA replication: positive or negative supercoiling?
Enzymes called topoisomerases supercoil DNA. There are two general classes of topoisomerases: topoisomerase I and topoisomerase II. Topoisomerase I enzymes are thought to mainly generate positive supercoils but can generate negative supercoils under certain conditions. Unlike topoisomerase II enzymes (see below), topoisomerase I enzymes are composed of a single protein subunit, do not use ATP during supercoiling, and only cut one of the two DNA strands during supercoil formation.
DNA gyrase from the bacterium E. coli is one of the best examples of a topoisomerase II enzyme. DNA gyrase uses the energy contained within ATP to introduce negative supercoils into chromosomes. Further, DNA gyrase is composed of four protein subunits, two A subunits and two B subunits.
Negative supercoils are generated by DNA gyrase using the following mechanism:
- The A subunits of DNA gyrase bind to the DNA.
- The A subunits function as an endonuclease to cut both strands of the DNA.
- The B subunits pass another portion of the DNA molecule through the break using the energy released by cleaving ATP.
- The DNA break is repaired producing an intact DNA double helix.
DNA gyrase generates two negative supercoils in the bacterial DNA per catalytic cycle; the production of each negative supercoil requires the cleavage of a single ATP molecule. For example, if the original bacterial DNA molecule had no supercoils, the same molecule would have two negative supercoils after DNA gyrase action (two ATP molecules consumed).
The ability to produce negative supercoils in the DNA is required for bacterial survival. A group of antibiotics called quinolones inhibit DNA gyrase, and therefore block bacterial growth. One example quinolone, ciprofloxacin, is used to treat patients infected with serious bacterial infections, including the bacterium that causes anthrax.
In bacteria, topoisomerase I and topoisomerase II compete to determine the overall level of supercoiling within the chromosome. Topoisomerase I and topoisomerase II enzymes also function in eukaryotic cells to help compact DNA.
- Describe how DNA gyrase introduces negative supercoils.
- What are some differences between the structure and function of DNA gyrase and topoisomerase I?
Eukaryotic Chromosome Compaction
Let us now consider how the human genome, which is over six feet in length, can be packaged into a single nucleus. Chromosome compaction in eukaryotes involves the association of the DNA double-helix with proteins (both histone and nonhistone proteins) to form chromatin.
The first level of chromosome compaction in eukaryotes involves the formation of structures called nucleosomes (see Figure 2.3). The basic structure of chromatin consists of chains of nucleosomes that resemble beads on a string. A nucleosome core particle consists of 146–147 base pairs (bp) of DNA negatively supercoiled around eight histone proteins. There are four types of histone proteins within a nucleosome; each histone protein is present in two copies. These histone proteins are called H2A, H2B, H3, and H4.
Each histone protein consists of a globular domain and an extended, flexible region called a histone tail. The globular domain allows the individual histone proteins to bind to each other to form nucleosomes, while the histone tails are rich in basic amino acids, such as arginine and lysine, and as a result, are positively charged. The backbone portion of the DNA double helix is negatively charged; thus, the histone tail and DNA backbone bind through electrostatic interactions to compact the chromosome.
Each nucleosome is connected by a linker region of between 20 and 100 bp of DNA. Histone H1, also called the linker histone, and other poorly defined nonhistone proteins bind to the linker region DNA. H1 and these nonhistone proteins play a role in further compaction of DNA into 30-nm fibers (see below).
- What is a nucleosome?
- What are the names of the protein components within a nucleosome?
- Explain how the DNA and histone proteins assemble to make a nucleosome.
- What is a linker region?
The second level of chromosome compaction in eukaryotes involves the association of a string of nucleosomes into a fiber that is 30 nanometers (nm) in width (30-nm fiber). The formation of the 30-nm fiber depends on the linker histone H1 and nonhistone proteins. Two general models have been proposed for the 30-nm fiber (see Figure 2.4):
- Solenoid. The solenoid involves the association of nucleosomes to form a compact, symmetrical structure that resembles a helix. The solenoid form of the 30-nm fiber is advantageous because it allows a high degree of chromosome compaction. However, genes within the solenoid are not accessible for transcription.
- Zigzag. In the zigzag, nucleosome interaction is minimal and the linker regions are free to bend and twist. The overall structure of the zigzag 30-nm fiber, as a result, is irregular. The zigzag form of the 30-nm fiber is advantageous because it promotes transcription, but the degree of chromosome compaction is not as great as with the solenoid form.
Recent evidence suggests that the zigzag form of the 30-nm fiber is found predominantly in cells; however, some scientists believe that the two forms of the 30-nm fiber can convert into each other depending on the needs of the cell.
- What are the advantages and disadvantages of the solenoid and zigzag models of the 30-nm fiber?
Radial Loop Domains (300-nm fibers)
The third level of DNA compaction in eukaryotes involves the interaction of the 30-nm fibers with a collection of proteins in the nucleus (nuclear matrix) to form structures called radial loop domains (see Figure 2.5). The eukaryotic radial loop domain is somewhat similar to the prokaryotic microdomain, with each radial loop consisting of 25,000–200,000 base pairs (bp) of DNA.
The nuclear matrix consists of two parts, the nuclear lamina and the internal nuclear matrix. The nuclear lamina is composed of cytoskeletal proteins called intermediate filaments and lies adjacent to the inner surface of the nuclear membrane. The internal nuclear matrix, which may include hundreds of different types of proteins, forms a fine meshwork of filaments throughout the interior of the nucleus.
Sequences within the DNA called matrix-attachment regions (MARs) link the 30-nm fiber to the internal nuclear matrix. Anchoring the 30-nm fiber to the internal nuclear matrix results in the formation of radial loop domains.
- What is a radial loop domain?
- How do the MARs and the internal nuclear matrix contribute to radial loop domain formation?
The internal nuclear matrix also functions to organize the chromosomes within the nucleus of a cell. Every chromosome is located within a unique region of the nucleus called a chromosome territory. These chromosome territories within the nucleus can be visualized when the individual chromosomes are labelled with uniquely colored fluorescent dyes (see Figures 2.5 and 2.6).
- What is a chromosome territory?
Heterochromatin and Euchromatin
The radial loop domains can assume two different conformations (see Figure 2.7):
- Euchromatin is a region of chromatin where the radial loops are not tightly compacted. Structural genes that are transcribed are typically found in euchromatin.
- Heterochromatin is defined as regions of the chromosome where the radial loops are tightly compacted. Most areas of heterochromatin either do not contain structural genes or the structural genes within these regions are not transcribed. There are two forms of heterochromatin:
- Constitutive heterochromatin. The centromere and the telomeres of chromosomes always assume the heterochromatin conformation and, are therefore, considered to be constitutive heterochromatin. Constitutive heterochromatin often contains repetitive DNA sequences (see Part 1).
- Facultative heterochromatin. Facultative heterochromatin is a dynamic structure that can convert between heterochromatin and euchromatin. For example, when one of the two X chromosomes in female mammals is chosen to be inactivated during early embryogenesis, the X chromosome is converted from euchromatin to heterochromatin (see below). The heterochromatin form of the X chromosome is called a Barr body. Further, each cell type in the body contains a unique pattern of facultative heterochromatin, meaning the distribution of facultative heterochromatin in a white blood cell is different from an epithelial cell. These differences in facultative heterochromatin ensure that each cell type transcribes a unique subset of genes. We will examine how changes in facultative heterochromatin influences gene activation in Parts 14 and 15.
- What is the difference between euchromatin and heterochromatin?
- How do the two types of heterochromatin differ from one another?
Nucleosomes, 30nm fibers, and radial loop domains are found in the chromatin of interphase cells. During mitosis and meiosis, the chromosomes become even more compacted, 10,000 times more compact than what is observed during interphase. In fact, the characteristic X-shaped chromosomes in mitosis and meiosis are composed mainly of heterochromatin. As a result, few structural genes are active during mitosis and meiosis.
To form highly compacted mitotic and meiotic chromosomes, the radial loops interact with a unique protein structure called the scaffold (see figure 2.8). The scaffold ensures that the radial loops throughout the majority of the chromosome are in the heterochromatin conformation. The structure of the scaffold is poorly understood; however, scientists believe the scaffold is composed of nonhistone proteins, including condensin (see below), and reorganized nuclear matrix proteins. The shape of metaphase chromosomes is due to radial loop domains binding to the scaffold.
- What are the four levels of chromosome compaction in eukaryotes?
- Which levels are compaction are observed during interphase?
- Which levels of compaction are observed during mitosis and meiosis?
The condensin protein plays an important role in the formation of mitotic and meiotic chromosomes. When a eukaryotic cell is in interphase, condensin is found in the cytoplasm of the cell. However, during mitosis and meiosis, the nuclear envelope breaks down and condensin can then bind to the chromosomes. Condensin is thought to link several radial loop domains together and hold them in place, forming heterochromatin.
Condensin is a member of a group of proteins called structural maintenance of chromosome (SMC) proteins. Recall that other members of the SMC family play a role in bacterial chromosome compaction (see above). All SMC proteins cleave ATP and use the released energy to promote changes in chromatin structure.
- How does condensin contribute to chromosome compaction?
B. X Chromosome Inactivation
Because female animals have two X chromosomes, females can potentially produce twice as much of the protein products from X-linked structural genes as their male counterparts who have a single X chromosome. However, we know that the level of X-linked protein production is similar between males and females.
This dosage compensation between males and females can be accomplished in several different ways. In mammals, one of the two X chromosomes is inactivated in females. For example, in humans, females randomly inactivate either the paternal or maternal X chromosome in somatic cells, while female marsupials inactivate the X chromosome they inherited from their father. Fruit flies conduct dosage compensation by increasing X-linked gene expression in males twofold. Finally, female nematode worms reduce gene expression on each X chromosome by 50% to accomplish dosage compensation.
- Why is dosage compensation important?
- How do humans accomplish dosage compensation?
Evidence for X Chromosome Inactivation (XCI)
In mammals, one of the X chromosomes is inactivated through a process called X chromosome inactivation (XCI). XCI was first suggested by two lines of experimental evidence:
- The studies of Murray Barr and Ewart Bertram. Barr and Bertram found that somatic cells from female cats contained a nuclear structure (a Barr body), not found in the males (see Figure 2.9). The Barr body is a highly condensed and inactive X chromosome; few structural genes (~15%) present within a Barr body are expressed.
- The studies of Mary Lyon. Female tortoiseshell and calico cats have a distinctive coat pattern, consisting of patches of orange and black fur. These cats with patches of orange and black fur are considered to be mosaics. The mosaic phenotype occurs in female cats that are heterozygous for X-linked coat color alleles (XbXo). The Xb allele is expressed in black patches, while the Xo allele is silenced. Similarly, the Xo allele is expressed in orange patches, while the Xb allele is silenced. Mary Lyon suggested that the mosaic calico pattern was due to XCI.
- How did the experiments by Barr, Bertram, and Lyon demonstrate that XCI occurs?
The Lyon Hypothesis
The Lyon Hypothesis, first proposed by Mary Lyon, provided a deeper understanding of XCI.
Consider the fur color trait in mice. Fur color is controlled by two X-linked alleles: The XB allele produces black fur color while the Xb produces white fur color. Suppose we have a heterozygous female mouse (XBXb), with a mosaic phenotype, similar to the tortoiseshell and calico cat coat patterns discussed above. The Lyon hypothesis states that during embryonic development in mice, both of the X chromosomes are active in each embryonic cell. However, one of the X chromosomes in each embryonic cell is soon inactivated and becomes a Barr body. This inactivation process is random in each embryonic cell, one cell may inactivate XB; a neighboring cell may inactivate Xb.
The embryonic cell containing an inactive XB allele continues to divide to produce a patch of cells where Xb is still active, resulting in white fur in that patch (see Figure 2.10). The embryonic cell containing an inactive Xb allele continues to divide to produce a patch of cells where XB is still active, resulting in black fur in that patch. Collectively, these events produce the mosaic phenotype of the heterozygous mouse.
One consequence of the Lyon hypothesis is that all female mammals (including humans) are thought to be mosaics if they are heterozygous for X-linked alleles. That means that in some areas of the body one X-linked allele is expressed; other areas of the body express the other X-linked allele. Anhidrotic ectodermal dysplasia is a human genetic disease caused by an X-linked recessive mutation. If a male possesses the recessive disease allele, he displays a variety of defects, including the absence of sweat glands. Heterozygous females are mosaics where some areas of the body have sweat glands; other areas lack sweat glands.
- What is the Lyon hypothesis and how does it explain the mosaic coat phenotypes seen in mice and cats?
X-inactivation Center (Xic)
In females with two X chromosomes, one X chromosome is inactivated to produce a Barr body. In Turner syndrome females with one X chromosome, Barr bodies are not observed. In Triplo-X syndrome females with three X chromosomes, two Barr bodies are formed; and in Klinefelter syndrome males with two X chromosomes and a Y chromosome, a single Barr body is formed. Thus, it appears that mammalian cells can “count” the number of X chromosomes in a particular cell and ensure that only one X chromosome remains active.
X chromosome inactivation is controlled by a region of the X chromosome, near the centromere, called the X-inactivation center (Xic). If the Xic is missing from one X chromosome and is present on the other X chromosome, then both X chromosomes remain active; two Xics must be present for one X chromosome to be inactivated. This provides evidence that it is not the X chromosomes that are counted by the cell, per se, but actually the number of Xics. If two or more Xics are present in a cell, only one remains active. The other Xics (and the X chromosomes) are inactivated.
- Why does the number of Barr bodies differ in genetic disorders of the X chromosome?
Xist and Tsix
The Xic region of the X chromosome contains two genes called Xist and Tsix (see figure 2.11).
- The Xist gene. Xist (X-inactive specific transcript) is a gene that is transcribed preferentially from the X chromosome that will be inactivated. The Xist gene produces a large RNA molecule that is an example of a non-coding RNA (ncRNA). Non-coding RNA molecules function directly in the cell and are not translated to make a protein product. The Xist RNA functions to recruit a variety of proteins that modify the structure of the X chromosome, converting an active X chromosome into a Barr body.
- The Tsix gene. The Tsix gene overlaps the Xist gene within the Xic and is transcribed in the opposite direction as the Xist gene. When the Tsix gene is transcribed, a ncRNA molecule called Tsix RNA is made. The Tsix RNA is transcribed from both X chromosomes prior to XCI and likely allows the two X chromosomes to pair briefly during early embryonic development (see Part 15). The Tsix RNA is later transcribed preferentially from the active X chromosome, which in turn inhibits Xist RNA production. Thus, the Xist RNA does not inactivate one X chromosome because on the active X chromosome, the Tsix gene is active. The production of the Tsix RNA inhibits the production of the Xist RNA from the X chromosome that will remain active.
- How does the Xist gene promote the formation of a Barr body?
- How does the Tsix gene ensure that one X chromosome remains active?
The Three Stages of XCI
The process of XCI has three stages (see Figure 2.12):
- The initiation stage involves a choice as to which X chromosome is inactivated. Tsix gene expression from the X chromosome that will remain active inhibits the production of the Xist RNA. The X chromosome that is inactivated does not express the Tsix RNA. As a result, the Xist RNA remains active and leads to the formation of a Barr body.
- The spreading stage involves the actual inactivation of one of the X chromosomes. The Xist RNA participates in spreading by starting at the Xic and coating the X chromosome to be inactivated in both directions. This coating with Xist RNA allows proteins to recognize the X chromosome and compact it to form a Barr body.
- Suppose a cell divides by mitosis. Prior to mitosis, this cell with an inactive X chromosome converts the Barr body into euchromatin and replicates the Barr body DNA. The replicated X chromosome is then separated into the daughter cells and is silenced again. Interestingly, the daughter cells have the ability to remember which X chromosome was inactivated in the parent cell prior to cell division. Thus, the two progeny cells both contain inactive copies of the same X chromosome as the parent cell. This stage is called maintenance.
- Explain the process of XCI in mammals, giving consideration to the three stages.
Fill in the blanks:
Chromosome Compaction Strategies in Prokaryotes and Eukaryotes
- _______________ are proteins that help compact the E. coli chromosome into microdomains.
- The enzyme ____________________ produces both positive and negative supercoiling.
- Topoisomerase _____ uses ATP to generate negative supercoils in bacterial chromosomes.
- Histone _____ is also called the linker because it links two nucleosomes together.
- A nucleosome contains ______________ bp of DNA wrapped around ___________ histone proteins.
- Amino acids _________ and __________ are positively charged, and make up many of the amino acids in the histone tail.
- The _________________ form of the 30-nm fiber resembles a helical structure.
- DNA sequences called _________________connect the 30-nm fiber to the internal nuclear matrix.
- ____________________ heterochromatin can be transcribed under certain cellular conditions.
- A region in the nucleus where a particular chromosome is located is called a chromosome ___________________.
- During interphase, condensin proteins are located in the _____________ of the cell.
X Chromosome Inactivation
- A normal female has _____ Barr body(bodies) whereas a female with Turner syndrome has _____ Barr body (bodies).
- When the Xist gene is active, it transcribes an RNA molecule that attaches to the chromosome that becomes (active or inactive). Circle the correct answer.
- When the Tsix gene is active, it transcribes an RNA molecule that is associated with the (active or inactive) X chromosome. Circle the correct answer.
- The inactive X chromosome condenses into a tight nuclear structure called a __________.
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