The English King, Richard III, was killed at the Battle of Bosworth on 22nd August 1485. Contemporary accounts reveal that he was fighting heroically while pressed on all sides by his enemies, the armed forces of the rebel Henry Tudor (later Henry VII). Famously (and possibly erroneously) depicted
by Shakespeare as a murderous, unscrupulous monster, Richard III was the last
English king to be killed in battle. So
why am I writing about a long-dead monarch in a forensics blog? Keep reading to find out!
An archaeological team from the University of Leicester, in association with Leicester City Council and the Richard III Society, has been excavating the site of a mediaeval Franciscan friary in Leicester called Grey Friars.
On September 12th 2012, while excavating the choir of Grey Friars church, which is believed to be the burial place of Richard III, archaeologists discovered a grave containing human remains.
Could
the remains be Richard III? We shan’t
know the answer, or even whether the question can be answered, until early in 2013. But forensic science is playing a key part in
the identification process.
Here
is the link to the most recent article on the discovery, which outlines the
scientific techniques being employed.
I
imagine that the ‘ancient DNA’ technique being used is Mitochondrial DNA
(mtDNA) analysis. Mitochondria (sing. Mitochondrion) are found in the cytoplasm
of cells i.e. outside the nucleus. They
are one of the most important ‘organelles’ of a cell, since they are the site
of the chemical reactions of respiration, whereby energy is generated for the
needs of the cell. A typical cell
contains about a thousand mitochondria.
Old bones,
badly decomposed or charred bodies are often poor sources of nuclear DNA, used
in standard DNA profiling. This is
because the nuclear DNA becomes degraded, chemically modified or contaminated,
and it is not possible to obtain a profile.
Mitochondrial DNA, although not immune to degradation, is better
protected within the cell than nuclear DNA.
Its extreme abundance means there is a much greater chance of some of it
surviving for longer.
Human
mtDNA is a circular molecule of DNA.
Most of it does not vary between individuals and therefore cannot be
used as a forensic identification tool.
However, in a region of the molecule called the ‘D Loop’ or ‘Control
Region’, variation does exist in DNA base sequences between unrelated
individuals, which is of forensic value.
I don’t
plan to go into the minutiae of the technique here, but I will mention an
important point about the inheritance of mtDNA.
All
brothers and sisters in a family will share the same mtDNA as their mother, but
not their father. They will also share
the same mtDNA as their mother’s siblings and their grandmother. This is because an individual inherits their
mtDNA only from their mother.
As a
consequence, mtDNA analysis cannot provide a unique identification because many
individuals can have the same mtDNA base sequences. Even between unrelated individuals, mtDNA
analysis is not as discriminating as standard DNA profiling. The process itself
is also not as straightforward as standard DNA profiling. But it can generate data when standard DNA
profiling fails, and this is the technique's undoubted advantage.
I’m
very interested to discover that a (male) potential descendant of Richard III’s sister
through the female line has been found, so that his mtDNA base sequences can be
compared with the base sequences that, hopefully, will be obtained from the
mtDNA of the remains.
It would be great if the scientific team are able to find sufficient evidence from their research
to suggest that the remains are Richard III. Follow me on Twitter @forensicswrite to find
out.