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Changing chromosome numbersMany people regard chromosome numbers in animals as being essentially fixed. While it is true that chromosome numbers are generally fairly stable within a population of animals, they are by no means completely static.
A karyotype from an individual with Down’s syndrome that resulted from a Robertsonian translocation. One copy of chromosome 21 is attached to one of chromosome 14 (the translocated chromosome) and two additional copies of chromosome 21 are present. About 5% of Down’s syndrome cases are the result of this type of translocation. The most common and best known chromosomal rearrangement affecting chromosome number is the Robertsonian translocation (ROB). It is named after the American geneticist W.R.B. Robertson, who first described this chromosomal rearrangement in grasshoppers in 1916. It occurs when the long arms of two acrocentric chromosomes (chromosomes with the centromere very near one end) fuse to form one metacentric chromosome (a chromosome with the centromere near the middle). The short arms of the original chromosomes are generally lost with no obvious adverse consequences.1 ROBs can be associated with problems. In humans, approximately one in 1,000 babies is born with this form of translocation.2 Most appear normal, though they may experience fertility problems later in life. Fertility problems can arise when gametes (egg or sperm) are formed that are missing or have extra chromosomes. Gametes from ROB carriers may be normal, with one of each chromosome or balanced, with the translocated chromosome but neither of the acrocentric homologues. However, on occasion unbalanced gametes may be formed that are either missing a chromosome or have the translocated chromosome with one of its acrocentric homologues. Unbalanced gametes can give rise to embryos which fail to develop or develop with abnormalities such as Down’s syndrome. It is estimated that 5% of Down’s syndrome cases are the result of an ROB. While it is true that chromosome numbers are generally fairly stable within a population of animals, they are by no means completely static. Although ROBs can be associated with problems, there are times where no adverse outcomes are observed. For example, they have been observed in Saanan goats with a normal phenotype and no reported fertility problems.3 There are crossbreeding studies with sheep carrying up to three different translocations that showed no significant effect on phenotype or fertility for any of the combinations.4 In fact, the normal chromosome number of domestic sheep (Ovis aries, 2n = 54) is inferred to be the result of three different translocations relative to domestic goats (Capra hircus, 2n = 60). The variation in chromosome number in the Bovidae family (including the tsoan5 and cattle6 monobaramins) appears to be mostly due to ROBs. There are other types of chromosomal rearrangements that have contributed to the range of chromosome numbers in animals that are monobaraminic (known to be from the same created kind). Some of these rearrangements are quite unexpected. For example, the Indian muntjac (Muntiacus muntjak, 2n = 6 in females, 7 in males) has the x-chromosome fused with one of its autosomes. The y-chromosome is separate. The male will have one of this autosomal pair fused to an x, and the other without a fused sex chromosome and a separate y, giving it an extra chromosome compared to the female. It is interesting to note that viable hybrids have been formed between this species and Reeve’s muntjac (Muntiacus reevesi, 2n = 46).7 Some species of antelope have a fused y-chromosome.8 ROBs have been shown to be non-random and appear to have distinct mechanisms governing their formation.9 They occur frequently enough without serious consequence to suggest that they serve some useful purpose. Much is unknown; particularly what factors influence their occurrence and what important results they may have. They are believed to have played a role in speciation within the family Bovidae. As further research reveals more information, it is likely we will find still another designed mechanism within the genome that points to an all-wise Creator. Further readingRelated resourcesReferences
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