variation in chromosome number

Variation in chromosome number

A summary of the terms used to describe heteroploidy (variation in chromosome number)
     

Term

Type of change

Symbol*

Heteroploid

Aneuploid
     

Nullisomic
Monosomic
Double trisomic

Trisomic
B. Euploid


Monoploid
Haploid
Polyploid

1. Autopolyploid

Autotriploid
Autotetraploid
Autopentaploid
Autohexaploid
Autooctaploid

  • Allopolyploid

Allotetraploid
Allohexaploid
Allooctaploid

A change from 2x
One or a few chromosomes extra or missing from 2n
One chromosome pair missing
One chromosome missing
One chromosome from each of two different chromosome pairs missing
One chromosome pair extra
Number of genomes or copies of a genome more than two
One copy of a single genome
Gametic chromosome complement
More than 2 copies of one genome or 2 copies each of 2 or more genomes**
Genomes identical with each other
Three copies of one genome
Four copies of one genome
Five copies of one genome
Six copies of one genome
Eight copies of one genome
Two or more distinct genomes (Generally each genome has two copies) **
Two distinct genomes
Three distinct genomes
Four distinct genomes

-
2n ±
few

2n-2
2n-1

2n-1-1

2n+2

x
n

3x
4x
5x
6x
8x

(2x1+2x2)**
(2x1+2x2+2x3)**
(2x1+2x2+2x3+2x4)**

  • *2n= Somatic chromosome number (and complement) and n= gametic chromosome number (and complement) of the species, whether diploid or polyplod.
  • X = The basic chromosome number (and complement) or genomic number.
  • x1,x2,x3,x4 = Distinct genomes from different species.
  • ** In general, this condition occurs; other situations may also occur.
  • A diploid in which 1 chromosome is missing from the total complement (2n-1) is known as monosomics. A double monosomic individual has two chromosomes missing, but the two chromosomes belong to two different chromosome pairs (2n-1-1). An individual having one extra chromosome (2n+1) is known as trisomic, and that having two extra chromosomes each belonging to a different chromosome pair is called double trisomic (2n+1+1). When an individual has an extra pair of chromosomes, it is known as tetrasomic (2n+2). The same is true about the various features of and the facts accumulated about aneuploidy as well as euploidy. The breeder is generally concerned with monosomics and trisomics, and, in some situations, with nullisomics and tetrasomics.
  • In euploids, the chromosome number is an exact multiple of the basic or genomic number. Euploidy is more commonly known as polyploidy. When all the genomes present in a polyploidy species are identical, it is known as autopolyploid and the situation is termed as autopolyploidy. In the case of allopolyploids, two or more distinct genomes are present. Euploids may have 3 (triploid), 4 (tetraploid), 5 (pentaploid), 6 (hexaploid), 7 (heptaploid), 8 (octaploid) or more genomes making up their somatic chromosomes number.
  • In case of autopolyploidy, they are known as autotriploid, autotertaploid, autopentaploid, autohexaploid, autoheptaploid, auto octaploid and so on, while in the case of allopolyploidy they are termed as allotriploid, allotetraploid, allopentaploid, allohexaploid, alloheptaploid, allooctaploid etc, Amphidiploid is an allopolyploid that has two copies of each genome present in it and, as a consequence, behaves as a diploid during meiosis. A segmental allopolyploid contains two or more genomes, which are identical with each other, except for some minor differences.


Last modified: Monday, 2 April 2012, 7:30 PM