The Boveri–Sutton chromosome theory (also known as the chromosome theory of inheritance or the Sutton–Boveri theory) is a fundamental unifying theory of genetics which identifies chromosomes as the carriers of genetic material.[1][2][3] It correctly explains the mechanism underlying the laws of Mendelian inheritance by identifying chromosomes with the paired factors (particles) required by Mendel's laws. It also states that chromosomes are linear structures with genes located at specific sites called loci along them.[2]
It states simply that chromosomes, which are seen in all dividing cells and pass from one generation to the next, are the basis for all genetic inheritance.
Over a period of time random mutation
creates changes in the DNA sequence of a gene. Genes are located on chromosomes.
Background
"1. The chromosome group of the presynaptic germ-cells is made up of two equivalent chromosome-series, and that strong ground exists for the conclusion that one of these is paternal and the other maternal.
2. The process of synapsis (pseudo-reduction) consists in the union in pairs of the homologous members (i. e., those that correspond in size) of the two series.
3. The first post-synaptic or maturation mitosis is equational and hence results in no chromosomic differentiation.
4. The second post-synaptic division is a reducing division, resulting in the separation of the chromosomes which have conjugated in synapsis, and their relegation to different germ-cells.
5. The chromosomes retain a morphological individuality throughout the various cell-divisions.
"
The chromosome theory of inheritance is credited to papers by Walter Sutton in 1902[5] and 1903,[6] as well as to independent work by Theodor Boveri during roughly the same period.[7] Boveri was studying sea urchins, in which he found that all the chromosomes had to be present for proper embryonic development to take place.[8] Sutton's work with grasshoppers showed that chromosomes occur in matched pairs of maternal and paternal chromosomes which separate during meiosis and "may constitute the physical basis of the Mendelian law of heredity".[9]
This groundbreaking work led E.B. Wilson in his classic text to name the chromosome theory of inheritance the "Sutton-Boveri Theory".[10] Wilson was close to both men since the young Sutton was his student and the prominent Boveri was his friend (in fact, Wilson dedicated the aforementioned book to Boveri). Although the naming precedence is now often reversed to "Boveri-Sutton", there are some who argue that Boveri did not actually articulate the theory until 1904.[11]
Verification
The proposal that chromosomes carried the factors of Mendelian inheritance was initially controversial, but in 1905 it gained
strong support when Nettie Stevens showed that the "accessory chromosome" of mealworms' sperm cells was decisive in the sex identity of the progeny,[12][13] a discovery supported by her mentor E.B. Wilson.[14] Later, Eleanor Carothers documented definitive evidence of independent assortment of chromosomes in a species of grasshopper.[15] Debate continued, however, until 1915 when Thomas Hunt Morgan's work on inheritance and genetic linkage in the fruit fly Drosophila melanogaster provided incontrovertible evidence for the proposal.[1][better source needed][3] The unifying theory stated that inheritance patterns may be generally explained by assuming that genes are located in specific sites on chromosomes.
^NM Stevens, (1905) “Studies in Spermatogenesis, with Especial Reference to the ‘Accessory Chromosome,’” Washington, DC, Carnegie Institution of Washington, Publication 36, NM Stevens, (1906) .
^
“Studies in Spermatogenesis Part II, A Comparative Study of Heterochromosomes in certain Species of Coleoptera, Hemiptera, and Lepidoptera with Especial Reference to Sex Determination,” Washington, DC, Carnegie Institution of Washington, Publication 36, Part II, (1906)