Ring chromosome
Chromosome whose ends have fused together to form a ring
From Wikipedia, the free encyclopedia
A ring chromosome is an aberrant chromosome whose ends have fused together to form a ring. Early observations of ring chromosomes were made during the development of cytogenetics in the early 20th century. Lilian Vaughan Morgan reported an unusual X chromosome in Drosophila melanogaster in 1926 that appeared “almost or entirely closed and somewhat rounded,” a structure later interpreted as a ring chromosome.[1] In 1930, Mikhail Sergeevich Navashin described chromosomes in species of Crepis whose ends had fused to form a closed ring, providing the first explicit cytological description of ring chromosomes in plants.[2] Barbara McClintock subsequently reported ring chromosomes in maize in 1931 and carried out detailed studies of their behavior and instability in plant cells.[3] Early cytological syntheses subsequently listed ring chromosomes in Crepis (Navashin, 1930), Drosophila (L. V. Morgan, 1933), and maize (McClintock, 1932).[4]
A ring chromosome is denoted by the symbol r in human genetics and R in Drosophila genetics. Ring chromosomes may form in cells following genetic damage by mutagens like radiation, but they may also arise spontaneously during development.
Formation
In order for a chromosome to form a ring, both ends of the chromosome are usually missing, enabling the broken ends to fuse together. In rare cases, the telomeres at the ends of a chromosome fuse without any loss of genetic material, which results in a normal phenotype.[5]
Complex rearrangements, including segmental microdeletions and microduplications, have been seen in numerous ring chromosomes, providing important clues regarding the mechanisms of their formation.[6]
Small supernumerary rings can also form, resulting in a partial trisomy.[7]
Ring chromosomes are unstable during cell division and can form interlocking or fused rings.[7]
Associated syndromes
Human genetic disorders can be caused by ring chromosome formation. Although ring chromosomes are very rare, they have been found in all human chromosomes. Symptoms seen in patients carrying ring chromosomes are more likely to be caused by the deletion of genes in the telomeric regions of affected chromosomes, rather than by the formation of a ring structure itself.[8] Almost all ring chromosome syndromes feature marked growth delay.[7]
Ring chromosomes can be inherited or sporadic. Mosaicism is common and affects the severity of the condition.[8] Location of fusion also affects severity due to loss of differing amounts of genetic material from the ends of chromosomes.
Disorders arising from the formation of a ring chromosome include:
| Chromosome | Typical features | Reference |
|---|---|---|
| Ring chromosome 1 | Microcephaly, facial abnormalities | [9][10] |
| Ring chromosome 2 | Small stature | [11][12][13][14] |
| Ring chromosome 3 | [15][16][17] | |
| Ring chromosome 4 | Craniofacial abnormalities | [18][19][20] |
| Ring chromosome 5 | [21][22][23] | |
| Ring chromosome 6 | Microcephaly, facial abnormalities, hand abnormalities | [24][25] |
| Ring chromosome 7 | Craniofacial abnormalities, speech deficits | [26][27][28] |
| Ring chromosome 8 | Craniofacial abnormalities, hydronephrosis, hand abnormalities | [29][30][31] |
| Ring chromosome 9 | Delayed growth, abnormal facial features, low muscle tone | [32][33][34] |
| Ring chromosome 10 | Delayed growth, facial dysmorphism, reproductive abnormalities | [35][36] |
| Ring chromosome 11 | [37][38] | |
| Ring chromosome 12 | Delayed growth, abnormal facial features, microcephaly | [39][40][41] |
| Ring chromosome 13 | Microcephaly, delayed growth, reproductive abnormalities | [42][43] |
| Ring chromosome 14 | Epilepsy, intellectual disability | [44][45] |
| Ring chromosome 15 | Growth delay, microcephaly, intellectual disability | [46][47][48] |
| Ring chromosome 16 | Microcephaly, growth delay, facial abnormalities | [49][50] |
| Ring chromosome 17 | [51][52] | |
| Ring chromosome 18 | Growth delay, facial abnormalities | [53][54] |
| Ring chromosome 19 | [55][56] | |
| Ring chromosome 20 | Epilepsy, abnormal facial features, growth delay | [57][58] |
| Ring chromosome 21 | Short stature, microcephaly, reproductive abnormalities | [59][60] |
| Ring chromosome 22 | Hypotonia, autistic-like behavior | [61][62] |
| Ring chromosome X | Turner syndrome | [citation needed] |
| Ring chromosome Y | [63][64] |