Flush sisters or flush brothers are not identical twins

Flush sisters or flush brothers are not identical twins

April 2019 – Issue 71

Many Wagyu breeders are amazed at at the physical diversity that can be seen between full sisters or full brothers that are produced from the same flush. This diversity is a result of genetic differences between embryos that is created by the unique sample of parental DNA in each egg and in each sperm that are brought together during fertilisation.

Genetic differences between embryos

The use of artificial breeding technologies, including the production of embryos through flushing and artificial insemination are common-place in the Wagyu industry.

Many Wagyu breeders are amazed at the physical diversity that can be seen between full sisters or full brothers that are produced from the same flush. This diversity is a result of genetic differences between embryos that is created by the unique sample of parental DNA in each egg and in each sperm that are brought together during fertilisation.

Identical twins are genetically identical, they form from a single fertilised egg splitting early in embryo development to form two identical copies, each with the same DNA.

Flush sisters or flush brothers are not identical twins. Flush sisters or brothers are no different to normal brothers or sisters, they are genetically different versions of the sire and dam’s DNA combining. Flush sisters or brothers share the same sire and dam, like any other naturally produced sister or brother. The only different is, that they are produced at the same point in time.

Each individual flush sibling is the product of a different sperm and different egg. Each sperm and each egg caries a different sample of sire or dam’s DNA. This is why there is genetic diversity between siblings and why flush siblings are no different to normal brothers or sisters.

Figure 1
Each calf receives one copy of each of 30 chromosomes from each parent (60 copies in total – 2 of each chromosome).

Flush sisters or flush brothers are not identical twins

Within Wagyu BREEDPLAN, flush siblings and full siblings produced through normal matings used to only have the same EBVs estimated for each sibling. These were based on the mid-parent values, basically 50% of the sire and 50% of the dam. Once performance records are added to BREEDPLAN, the EBVs for full siblings would then change to reflect the phenotype differences observed by breeders.

Now that we have Single-Step Wagyu BREEDPLAN, including genomic information (50K SNP data) on flush siblings at registration we can tell exactly which DNA came from each parent and what the relative value of this DNA for each trait is in each of the progeny.

This means that genomics in BREEDPLAN can estimate the genetic difference between full siblings (including flush siblings) early on in life so that the genetic difference between siblings can be used within management and breeding decisions on-farm. The EBVs for full siblings can vary greatly depending on the relative merit of the genes they received from the parents.

To understand how this genetic diversity occurs between siblings, we need to understand the mechanism through which the diversity is created within the sex cells (sperm and eggs) of an animal.

Genetic Material

Chromosomes are the cellular structures that maintain and transmit genetic information. They are made of deoxyribonucleic acid (DNA) combined with proteins. The DNA provides the blueprint for the physical, and some of the behavioural, traits of the animal. These traits are a unique and random mix of the parents determined by which particular sperm happens to fertilise which particular egg.

Chromosome pairs

Every cell in cattle (except the gametes) contains 30 chromosome pairs or 60 chromosomes in total. The 60 chromosomes represent one copy of each chromosome from each parent.

Sex cells – the gametes

Gametes are special cells that have undergone reduction and contain only 30 chromosomes (one copy of each chromosome). These gametes are the female egg and the male sperm that fuse together during fertilisation, restoring the 60 chromosomes in the fertilised cell and initiating the events that result in embryo development.

Creation of Sex Cells (Meiosis)

Meiosis is the process that creates the gametes within the sperm and the egg of each of the parents. Meiosis occurs in two stages. In meiosis stage 1, the two copies of 30 chromosomes are sorted into two groups. The cell nucleus then dissolves and the 30 pairs of chromosomes line up along the centre of the cell. Some pair members from each parent exchange portions of their DNA in a process called crossover that helps increase genetic diversity by creating non-identical pairs. See Figure 2.

Following crossover, one copy of each chromosome pair is pulled to one side of the cell while the other copy is dragged to the opposite side (see figure 3). This process (also called independent assortment) occurs randomly to separate the chromosome pairs to opposite ends of the cell. A gamete will therefore end up with the full 30 chromosomes, but each gamete will have one of many different combinations of chromosomes and crossover chromosomes from the original set of 60.

This reshuffling of genes into unique combinations increases the genetic variation in a population and explains the variation we see between siblings with the same parents.

The halving of the number of chromosomes in gametes ensures that, after fertilisation, the embryo will have the same number of chromosomes as the parents (30 come from each parent gamete to make the 60 in total). This is critical for stable sexual reproduction through successive generations.

Figure 2
An example of the crossing over between the pairs of chromosomes for chromosome three. The above is only to illustrate the principle and crossing over normally occurs between several of the chromosome pairs during meiosis.

Flush sisters or flush brothers are not identical twins

Figure 3
One chromosome of each pair is dragged to each side, halving the number of chromosomes in each cell. Independent assortment caused black chromosome 28 and (mainly pink) chromosome 3 to be dragged to the top cell.

Flush sisters or flush brothers are not identical twins

To further genetic diversity, another round of meiosis occurs – meiosis stage 2. The chromosomes once again align at the centre of the cell. This time, the single-copy of chromosomes are distributed to two daughter cells known as gametocytes. In this way, one cell results in four non-identical gametocytes that undergo further development to become sperm or eggs.
See figure 4.

Figure 4
After meiosis finished 1 cell resulted in four non-identical sperm or egg cells.

Flush sisters or flush brothers are not identical twins

Figure 5 shows the impact of 50K genomics data on the EBVs of 7 flush siblings. In Wagyu BREEDPLAN pre-genomics, all 7 had the same Marble Score EBV, but due to weight data being provided during early life growth, the animals had different Carcase Weight EBVs.

Once 50K genomic data was added, Wagyu BREEDPLAN could determine the relative genetic merit of each individual for Marble Score, with large genetic variation now evident in this trait.

Flush sisters or flush brothers are not identical twins

Figure 5
A story of 7 full-flush siblings – the use of genomics clearly shows the effect on EBVs.

Important Notice and Disclaimer


It is very important that you appreciate when viewing the AWA database that the information contained on the AWA database, including but not limited to pedigree, DNA information, Estimated Breeding Values (EBVs) and Index values, is based on data supplied by members and/or third parties.

Whilst every effort is made to ensure the accuracy of the information reported through AWA, AWA officers and employees assume no responsibility for its content, use or interpretation. AWA disclaims all liability (including without limitation, liability in negligence) for all expenses, losses, damages and costs you may incur as a result of the use by you of the data on this AWA database and the information supplied by ABRI and AGBU being inaccurate or incomplete in any way for any reason.

Regarding EBVs and Index values, it is very important to appreciate, and you need to be aware that:

  • EBVs are derived using Wagyu Single Step BREEDPLAN technology developed independently by the Animal Genetics and Breeding Unit (AGBU), using the information contained within the AWA database.
  • AGBU is a joint venture of NSW Department of Primary Industries and the University of New England, which receives funding for this purpose from Meat and Livestock Australia Limited.
  • AWA relies solely on advice provided by AGBU and ABRI in accepting Wagyu Single Step BREEDPLAN software.
  • EBVs published in Wagyu Single Step BREEDPLAN are estimates of genetic potential of individual animals and may not reflect the raw animal phenotype.
  • EBVs can only be directly compared to other EBVs calculated in the same monthly Wagyu Group BREEDPLAN analysis.

Regarding pedigree and DNA testing results submitted to the AWA, it is very important to appreciate, and you need to be aware that:

  • Pedigree and DNA data submitted and supplied to AWA may have errors in it which cannot be detected without further DNA testing.
  • Technology may have advanced since a particular test was undertaken so that previous inaccuracies which were not detectable are now able to be detected by current testing technology.
  • AWA estimates that less than 1% of the pedigree entries, ownership or breeding details in the AWA Herdbook may have errors or which may be misleading. For this reason, users ought to consider if they need to obtain independent testing of the relevant animal (if possible) to ensure that the data is accurate.

Regarding prefectural content, it is very important to appreciate, and you need to be aware that:

  • Prefectural content is based on the estimation of prefectural origin from Japanese breeding records of 201 foundation sires and 168 foundation dams.  As genotype-based parent verification is not used in Japan, and full Japanese registration certificates are not available for all foundation animals, exact prefectural composition for these sires and dams cannot be validated.
  • The calculation of prefectural content for Australian Herdbook animals relies on the accuracy of pedigree records and DNA samples provided by AWA members.
  • The reporting of prefectural content for animals within the AWA Herdbook relies on the calculation provided by ABRI.

If you consider that you do not understand or appreciate the nature and extent of the data provided on this website or the EBVs of a particular animal, then AWA strongly recommends that you seek independent expert advice.