Chromosome

Diagram of a replicated and condensed metaphase eukaryotic chromosome. (1) Chromatid – one of the two identical parts of the chromosome after S phase. (2) Centromere – the point where the two chromatids touch. (3) Short strand. (4) Long strand.

A chromosome (from ancient Greek: χρωμόσωμα, chromosoma, chroma means color, soma means body) is a DNA molecule with part or all of the genetic material (genome) of an organism.

Chromosomes are normally visible under a light microscope only when the cell is undergoing the metaphase of cell division. Before this happens, every chromosome is copied once (S phase), and the copy is joined to the original by a centromere, resulting in an X-shaped structure. The original chromosome and the copy are now called sister chromatids. During metaphase, when a chromosome is in its most condensed state, the X-shape structure is called a metaphase chromosome. In this highly condensed form chromosomes are easiest to distinguish and study.[1]

Chromosomes vary widely between different organisms. Some species such as certain bacteria, which lack histones, also contain plasmids or other extrachromosomal DNA. These are circular structures in the cytoplasm that contain cellular DNA and play a role in horizontal gene transfer.[1] In prokaryotes (see nucleoids) and viruses,[2] the DNA is often densely packed and organized; in the case of archaea, by homology to eukaryotic histones, and in the case of bacteria, by histone-like proteins.

Compaction of the duplicated chromosomes during cell division (mitosis or meiosis) results either in a four-arm structure (pictured to the right) if the centromere is located in the middle of the chromosome or a two-arm structure if the centromere is located near one of the ends. Chromosomal recombination during meiosis and subsequent sexual reproduction play a significant role in genetic diversity. If these structures are manipulated incorrectly, through processes known as chromosomal instability and translocation, the cell may undergo mitotic catastrophe and die, or it may unexpectedly evade apoptosis, leading to the progression of cancer.

Some use the term chromosome in a wider sense, to refer to the individualized portions of chromatin in cells, either visible or not under light microscopy. However, others use the concept in a narrower sense, to refer to the individualized portions of chromatin during cell division, visible under light microscopy due to high condensation.

History of discovery

Walter Sutton (left) and Theodor Boveri (right) independently developed the chromosome theory of inheritance in 1902.

The word chromosome (/ˈkroʊməˌsoʊm, -ˌzoʊm/[3][4]) comes from the Greek χρῶμα (chroma, "colour") and σῶμα (soma, "body"), describing their strong staining by particular dyes.[5]

Schleiden,[1] Virchow and Bütschli were among the first scientists who recognized the structures now familiar as chromosomes.[6] The term was coined by von Waldeyer-Hartz,[7] referring to the term chromatin, which was introduced by Walther Flemming.

In a series of experiments beginning in the mid-1880s, Theodor Boveri gave the definitive demonstration that chromosomes are the vectors of heredity. His two principles were the continuity of chromosomes and the individuality of chromosomes. It is the second of these principles that was so original. Wilhelm Roux suggested that each chromosome carries a different genetic load. Boveri was able to test and confirm this hypothesis. Aided by the rediscovery at the start of the 1900s of Gregor Mendel's earlier work, Boveri was able to point out the connection between the rules of inheritance and the behaviour of the chromosomes. Boveri influenced two generations of American cytologists: Edmund Beecher Wilson, Nettie Stevens, Walter Sutton and Theophilus Painter were all influenced by Boveri (Wilson, Stevens, and Painter actually worked with him).[8]

In his famous textbook The Cell in Development and Heredity, Wilson linked together the independent work of Boveri and Sutton (both around 1902) by naming the chromosome theory of inheritance the Boveri–Sutton chromosome theory (the names are sometimes reversed).[9] Ernst Mayr remarks that the theory was hotly contested by some famous geneticists: William Bateson, Wilhelm Johannsen, Richard Goldschmidt and T.H. Morgan, all of a rather dogmatic turn of mind. Eventually, complete proof came from chromosome maps in Morgan's own lab.[10]

The number of human chromosomes was published in 1923 by Theophilus Painter. By inspection through the microscope, he counted 24 pairs, which would mean 48 chromosomes. His error was copied by others and it was not until 1956 that the true number, 46, was determined by Indonesia-born cytogeneticist Joe Hin Tjio.[11]

Prokaryotes

The prokaryotes – bacteria and archaea – typically have a single circular chromosome, but many variations exist.[12] The chromosomes of most bacteria, which some authors prefer to call genophores, can range in size from only 130,000 base pairs in the endosymbiotic bacteria Candidatus Hodgkinia cicadicola[13] and Candidatus Tremblaya princeps,[14] to more than 14,000,000 base pairs in the soil-dwelling bacterium Sorangium cellulosum.[15] Spirochaetes of the genus Borrelia are a notable exception to this arrangement, with bacteria such as Borrelia burgdorferi, the cause of Lyme disease, containing a single linear chromosome.[16]

Structure in sequences

Prokaryotic chromosomes have less sequence-based structure than eukaryotes. Bacteria typically have a one-point (the origin of replication) from which replication starts, whereas some archaea contain multiple replication origins.[17] The genes in prokaryotes are often organized in operons, and do not usually contain introns, unlike eukaryotes.

Structure of chromosome:

  1. Each chromosome is made up of two chromatids(chromosomal arms) which are joined to each other at a small constricted region called the centromere.(Primary constriction).
  2. The centromere helps the chromatids to get attached to the spindle fibres during cell division, it is also concerned with the anaphase movement of the chromosomes, by which the spindle fibers pull the chromatids to the two opposite poles by their contraction during anaphase.
  3. Besides the primary constriction, in certain chromosomes there is a secondary constriction as well. Because a the small portion is pinched off from the chromosomal body; this portion is called a 'satellite' and the chromosome is called an SAT chromosome.
  4. The two chromatids are made up of very thin chromatin fibres which are made up of 40% DNA and 60% histone proteins
  5. Each chromatin fibre consists of one DNA strand coiled around eight histone molecules like a loop; such a complex is called nucleosome.
  6. The primary constriction is a non-stainable region; during cell division this region appears like a gap.
  7. Within the primary constriction there is a clear zone called Centromere.
  8. The centromere with the DNA and histone proteins bound to them form a disc shaped structure called kinetochore.
  9. the chromonemata represents a chromatid in the early stage of condensation.

DNA packaging

Prokaryotes do not possess nuclei. Instead, their DNA is organized into a structure called the nucleoid.[18][19] The nucleoid is a distinct structure and occupies a defined region of the bacterial cell. This structure is, however, dynamic and is maintained and remodeled by the actions of a range of histone-like proteins, which associate with the bacterial chromosome.[20] In archaea, the DNA in chromosomes is even more organized, with the DNA packaged within structures similar to eukaryotic nucleosomes.[21][22]

Bacterial chromosomes tend to be tethered to the plasma membrane of the bacteria. In molecular biology application, this allows for its isolation from plasmid DNA by centrifugation of lysed bacteria and pelleting of the membranes (and the attached DNA).

Prokaryotic chromosomes and plasmids are, like eukaryotic DNA, generally supercoiled. The DNA must first be released into its relaxed state for access for transcription, regulation, and replication.

Eukaryotes

Organization of DNA in a eukaryotic cell.

In eukaryotes, nuclear chromosomes are packaged by proteins into a condensed structure called chromatin. This allows the very long DNA molecules to fit into the cell nucleus. The structure of chromosomes and chromatin varies through the cell cycle. Chromosomes are even more condensed than chromatin and are an essential unit for cellular division. Chromosomes must be replicated, divided, and passed successfully to their daughter cells so as to ensure the genetic diversity and survival of their progeny. Chromosomes may exist as either duplicated or unduplicated. Unduplicated chromosomes are single double helixes, whereas duplicated chromosomes contain two identical copies (called chromatids or sister chromatids) joined by a centromere.

The major structures in DNA compaction: DNA, the nucleosome, the 10 nm "beads-on-a-string" fibre, the 30 nm fibre and the metaphase chromosome.

Eukaryotes (cells with nuclei such as those found in plants, fungi, and animals) possess multiple large linear chromosomes contained in the cell's nucleus. Each chromosome has one centromere, with one or two arms projecting from the centromere, although, under most circumstances, these arms are not visible as such. In addition, most eukaryotes have a small circular mitochondrial genome, and some eukaryotes may have additional small circular or linear cytoplasmic chromosomes.

In the nuclear chromosomes of eukaryotes, the uncondensed DNA exists in a semi-ordered structure, where it is wrapped around histones (structural proteins), forming a composite material called chromatin.

Chromatin

Chromatin is the complex of DNA and protein found in the eukaryotic nucleus, which packages chromosomes. The structure of chromatin varies significantly between different stages of the cell cycle, according to the requirements of the DNA.

Interphase chromatin

During interphase (the period of the cell cycle where the cell is not dividing), two types of chromatin can be distinguished:

Metaphase chromatin and division

Human chromosomes during metaphase

In the early stages of mitosis or meiosis (cell division), the chromatin double helix become more and more condensed. They cease to function as accessible genetic material (transcription stops) and become a compact transportable form. This compact form makes the individual chromosomes visible, and they form the classic four arm structure, a pair of sister chromatids attached to each other at the centromere. The shorter arms are called p arms (from the French petit, small) and the longer arms are called q arms (q follows p in the Latin alphabet; q-g "grande"; alternatively it is sometimes said q is short for queue meaning tail in French[23]). This is the only natural context in which individual chromosomes are visible with an optical microscope.

Mitotic metaphase chromosomes are best described by a linearly organized longitudinally compressed array of consecutive chromatin loops.[24]

During mitosis, microtubules grow from centrosomes located at opposite ends of the cell and also attach to the centromere at specialized structures called kinetochores, one of which is present on each sister chromatid. A special DNA base sequence in the region of the kinetochores provides, along with special proteins, longer-lasting attachment in this region. The microtubules then pull the chromatids apart toward the centrosomes, so that each daughter cell inherits one set of chromatids. Once the cells have divided, the chromatids are uncoiled and DNA can again be transcribed. In spite of their appearance, chromosomes are structurally highly condensed, which enables these giant DNA structures to be contained within a cell nucleus.

Human chromosomes

Chromosomes in humans can be divided into two types: autosomes (body chromosome(s)) and allosome (sex chromosome(s)). Certain genetic traits are linked to a person's sex and are passed on through the sex chromosomes. The autosomes contain the rest of the genetic hereditary information. All act in the same way during cell division. Human cells have 23 pairs of chromosomes (22 pairs of autosomes and one pair of sex chromosomes), giving a total of 46 per cell. In addition to these, human cells have many hundreds of copies of the mitochondrial genome. Sequencing of the human genome has provided a great deal of information about each of the chromosomes. Below is a table compiling statistics for the chromosomes, based on the Sanger Institute's human genome information in the Vertebrate Genome Annotation (VEGA) database.[25] Number of genes is an estimate, as it is in part based on gene predictions. Total chromosome length is an estimate as well, based on the estimated size of unsequenced heterochromatin regions.

Chromosome Genes[26] Total base pairs % of bases Sequenced base pairs[27]
1 2000 247,199,719 8.0 224,999,719
2 1300 242,751,149 7.9 237,712,649
3 1000 199,446,827 6.5 194,704,827
4 1000 191,263,063 6.2 187,297,063
5 900 180,837,866 5.9 177,702,766
6 1000 170,896,993 5.5 167,273,993
7 900 158,821,424 5.2 154,952,424
8 700 146,274,826 4.7 142,612,826
9 800 140,442,298 4.6 120,312,298
10 700 135,374,737 4.4 131,624,737
11 1300 134,452,384 4.4 131,130,853
12 1100 132,289,534 4.3 130,303,534
13 300 114,127,980 3.7 95,559,980
14 800 106,360,585 3.5 88,290,585
15 600 100,338,915 3.3 81,341,915
16 800 88,822,254 2.9 78,884,754
17 1200 78,654,742 2.6 77,800,220
18 200 76,117,153 2.5 74,656,155
19 1500 63,806,651 2.1 55,785,651
20 500 62,435,965 2.0 59,505,254
21 200 46,944,323 1.5 34,171,998
22 500 49,528,953 1.6 34,893,953
X (sex chromosome) 800 154,913,754 5.0 151,058,754
Y (sex chromosome) 50 57,741,652 1.9 25,121,652
Total 21,000 3,079,843,747 100.0 2,857,698,560

Number in various organisms

In eukaryotes

These tables give the total number of chromosomes (including sex chromosomes) in a cell nucleus. For example, human cells are diploid and have 22 different types of autosome, each present as two copies, and two sex chromosomes. This gives 46 chromosomes in total. Other organisms have more than two copies of their chromosome types, such as bread wheat, which is hexaploid and has six copies of seven different chromosome types – 42 chromosomes in total.

Chromosome numbers in some plants
Plant Species #
Arabidopsis thaliana (diploid)[28] 10
Rye (diploid)[29] 14
Einkorn wheat (diploid)[30] 14
Maize (diploid or palaeotetraploid)[31] 20
Durum wheat (tetraploid)[30] 28
Bread wheat (hexaploid)[30] 42
Adder's tongue fern (diploid)[32] approx. 1,200
Chromosome numbers (2n) in some animals
Species #
Common fruit fly 8
Pill millipede (Arthrosphaera fumosa)[33] 30
Earthworm (Octodrilus complanatus)[34] 36
Tibetan fox 36
Domestic cat[35] 38
Domestic pig 38
Laboratory mouse[36][37] 40
Laboratory rat[37] 42
Rabbit (Oryctolagus cuniculus)[38] 44
Syrian hamster[36] 44
Guppy (poecilia reticulata)[39] 46
Human[40] 46
Hares[41][42] 48
Gorillas, chimpanzees[40] 48
Domestic sheep 54
Garden snail[43] 54
Silkworm[44] 56
Elephants[45] 56
Cow 60
Donkey 62
Guinea pig[46] 64
Horse 64
Dog[47] 78
Hedgehog 90
Goldfish[48] 100-104
Kingfisher[49] 132
Chromosome numbers in other organisms
Species Large
Chromosomes 		Intermediate
Chromosomes 		Microchromosomes
Trypanosoma brucei 11 6 ~100
Domestic pigeon
(Columba livia domestics)[50] 		18 - 59-63
Chicken[51] 8 2 sex chromosomes 60

Normal members of a particular eukaryotic species all have the same number of nuclear chromosomes (see the table). Other eukaryotic chromosomes, i.e., mitochondrial and plasmid-like small chromosomes, are much more variable in number, and there may be thousands of copies per cell.

The 23 human chromosome territories during prometaphase in fibroblast cells.

Asexually reproducing species have one set of chromosomes that are the same in all body cells. However, asexual species can be either haploid or diploid.

Sexually reproducing species have somatic cells (body cells), which are diploid [2n] having two sets of chromosomes (23 pairs in humans with one set of 23 chromosomes from each parent), one set from the mother and one from the father. Gametes, reproductive cells, are haploid [n]: They have one set of chromosomes. Gametes are produced by meiosis of a diploid germ line cell. During meiosis, the matching chromosomes of father and mother can exchange small parts of themselves (crossover), and thus create new chromosomes that are not inherited solely from either parent. When a male and a female gamete merge (fertilization), a new diploid organism is formed.

Some animal and plant species are polyploid [Xn]: They have more than two sets of homologous chromosomes. Plants important in agriculture such as tobacco or wheat are often polyploid, compared to their ancestral species. Wheat has a haploid number of seven chromosomes, still seen in some cultivars as well as the wild progenitors. The more-common pasta and bread wheat types are polyploid, having 28 (tetraploid) and 42 (hexaploid) chromosomes, compared to the 14 (diploid) chromosomes in the wild wheat.[52]

In prokaryotes

Prokaryote species generally have one copy of each major chromosome, but most cells can easily survive with multiple copies.[53] For example, Buchnera, a symbiont of aphids has multiple copies of its chromosome, ranging from 10–400 copies per cell.[54] However, in some large bacteria, such as Epulopiscium fishelsoni up to 100,000 copies of the chromosome can be present.[55] Plasmids and plasmid-like small chromosomes are, as in eukaryotes, highly variable in copy number. The number of plasmids in the cell is almost entirely determined by the rate of division of the plasmid – fast division causes high copy number.

Karyotype

Karyogram of a human male

In general, the karyotype is the characteristic chromosome complement of a eukaryote species.[56] The preparation and study of karyotypes is part of cytogenetics.

Although the replication and transcription of DNA is highly standardized in eukaryotes, the same cannot be said for their karyotypes, which are often highly variable. There may be variation between species in chromosome number and in detailed organization. In some cases, there is significant variation within species. Often there is:

1. variation between the two sexes
2. variation between the germ-line and soma (between gametes and the rest of the body)
3. variation between members of a population, due to balanced genetic polymorphism
4. geographical variation between races
5. mosaics or otherwise abnormal individuals.

Also, variation in karyotype may occur during development from the fertilized egg.

The technique of determining the karyotype is usually called karyotyping. Cells can be locked part-way through division (in metaphase) in vitro (in a reaction vial) with colchicine. These cells are then stained, photographed, and arranged into a karyogram, with the set of chromosomes arranged, autosomes in order of length, and sex chromosomes (here X/Y) at the end.

Like many sexually reproducing species, humans have special gonosomes (sex chromosomes, in contrast to autosomes). These are XX in females and XY in males.

Historical note

Investigation into the human karyotype took many years to settle the most basic question: How many chromosomes does a normal diploid human cell contain? In 1912, Hans von Winiwarter reported 47 chromosomes in spermatogonia and 48 in oogonia, concluding an XX/XO sex determination mechanism.[57] Painter in 1922 was not certain whether the diploid number of man is 46 or 48, at first favouring 46.[58] He revised his opinion later from 46 to 48, and he correctly insisted on humans having an XX/XY system.[59]

New techniques were needed to definitively solve the problem:

  1. Using cells in culture
  2. Arresting mitosis in metaphase by a solution of colchicine
  3. Pretreating cells in a hypotonic solution 0.075 M KCl, which swells them and spreads the chromosomes
  4. Squashing the preparation on the slide forcing the chromosomes into a single plane
  5. Cutting up a photomicrograph and arranging the result into an indisputable karyogram.

It took until 1954 before the human diploid number was confirmed as 46.[60][61] Considering the techniques of Winiwarter and Painter, their results were quite remarkable.[62] Chimpanzees, the closest living relatives to modern humans, have 48 chromosomes as do the other great apes: in humans two chromosomes fused to form chromosome 2.

(See Also: Argument from authority#Inaccurate chromosome number)

Aberrations

In Down syndrome, there are three copies of chromosome 21

Chromosomal aberrations are disruptions in the normal chromosomal content of a cell and are a major cause of genetic conditions in humans, such as Down syndrome, although most aberrations have little to no effect. Some chromosome abnormalities do not cause disease in carriers, such as translocations, or chromosomal inversions, although they may lead to a higher chance of bearing a child with a chromosome disorder. Abnormal numbers of chromosomes or chromosome sets, called aneuploidy, may be lethal or may give rise to genetic disorders.[63] Genetic counseling is offered for families that may carry a chromosome rearrangement.

The gain or loss of DNA from chromosomes can lead to a variety of genetic disorders. Human examples include:

Sperm aneuploidy

Exposure of males to certain lifestyle, environmental and/or occupational hazards may increase the risk of aneuploid spermatozoa.[67] In particular, risk of aneuploidy is increased by tobacco smoking,[68][69] and occupational exposure to benzene,[70] insecticides,[71][72] and perfluorinated compounds.[73] Increased aneuploidy is often associated with increased DNA damage in spermatozoa.

See also

Notes and references

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  2. ↑ Johnson, J.; Chiu, W. (1 April 2000). "Structures of virus and virus-like particles". Current Opinion in Structural Biology. 10 (2): 229–235. PMID 10753814. doi:10.1016/S0959-440X(00)00073-7.
  3. ↑ Jones, Daniel (2003) [1917], Peter Roach, James Hartmann and Jane Setter, eds., English Pronouncing Dictionary, Cambridge: Cambridge University Press, ISBN 3-12-539683-2
  4. ↑ "Chromosome". Merriam-Webster Dictionary.
  5. ↑ Coxx, H. J. (1925). Biological Stains - A Handbook on the Nature and Uses of the Dyes Employed in the Biological Laboratory. Commission on Standardization of Biological Stains.
  6. ↑ Fokin S.I. (2013). "Otto Bütschli (1848–1920) Where we will genuflect?" (PDF). Protistology. 8 (1): 22–35.
  7. ↑ Waldeyer-Hartz (1888). "Über Karyokinese und ihre Beziehungen zu den Befruchtungsvorgängen". Archiv für mikroskopische Anatomie und Entwicklungsmechanik. 32: 27.
  8. ↑ Carlson, Elof A. (2004). Mendel's Legacy: The Origin of Classical Genetics (PDF). Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press. p. 88. ISBN 978-087969675-7.
  9. ↑ Wilson, E.B. (1925). The Cell in Development and Heredity, Ed. 3. Macmillan, New York. p. 923.
  10. ↑ Mayr, E. (1982). The growth of biological thought. Harvard. p. 749.
  11. ↑ Matthews, Robert. "The bizarre case of the chromosome that never was" (PDF). Archived from the original (PDF) on 15 December 2013. Retrieved 13 July 2013.
  12. ↑ Thanbichler M; Shapiro L (2006). "Chromosome organization and segregation in bacteria". J. Struct. Biol. 156 (2): 292–303. PMID 16860572. doi:10.1016/j.jsb.2006.05.007.
  13. ↑ Van Leuven, JT; Meister, RC; Simon, C; McCutcheon, JP (11 September 2014). "Sympatric speciation in a bacterial endosymbiont results in two genomes with the functionality of one.". Cell. 158 (6): 1270–80. PMID 25175626. doi:10.1016/j.cell.2014.07.047.
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  19. ↑ Le TB, Imakaev MV, Mirny LA, Laub MT (2013). "High-resolution mapping of the spatial organization of a bacterial chromosome". Science. 342 (6159): 731–4. PMC 3927313 Freely accessible. PMID 24158908. doi:10.1126/science.1242059.
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  25. ↑ Vega.sanger.ad.uk, all data in this table was derived from this database, November 11, 2008.
  26. ↑ "Ensembl genome browser 71: Homo sapiens – Chromosome summary – Chromosome 1: 1–1,000,000". apr2013.archive.ensembl.org. Retrieved 2016-04-11.
  27. ↑ Sequenced percentages are based on fraction of euchromatin portion, as the Human Genome Project goals called for determination of only the euchromatic portion of the genome. Telomeres, centromeres, and other heterochromatic regions have been left undetermined, as have a small number of unclonable gaps. See http://www.ncbi.nlm.nih.gov/genome/seq/ for more information on the Human Genome Project.
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  37. 1 2 Painter, TS (1928). "A Comparison of the Chromosomes of the Rat and Mouse with Reference to the Question of Chromosome Homology in Mammals". Genetics. 13 (2): 180–9. PMC 1200977 Freely accessible. PMID 17246549.
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