Poaceae Terminology
DNA Sequencing Technology
Poaceae Terminology
Tiller
Culm
Node
Internode
Intercallary meristem
Sheath
Open sheath
Closed sheath
Blade
Ligule
Auricle
Stolon
Rhizome
Inflorescence
Spike
Panicle
Panicle branch
Spikelet
Floret
Glume
Lemma
Palea
Rachilla
Rachis
Lodicule
Filament
Anther
Stigma
Caryopsis
DNA Sequencing Technology
Types of DNA:
There are three types of DNA that may be studied in plants, chloroplast DNA
(cDNA), mitochondrial DNA (mDNA) and nuclear DNA (nuclear chromosomes).
Nuclear DNA comprises the chromosomes of organisms. Each chromosome consists of one long, double-stranded DNA molecule with many genes located along its length. It tends to be highly repetitive, meaning there are many segments that are repeated many times throughout the chromosomes. Because most plants are polyploids, there also may be several copies of each chromosome present in every cell. Also, there may be segments of DNA that are never expressed in the plant.
Chloroplast DNA is found in chloroplasts only. Chloroplasts may represent an ancient symbiotic relationship between photosynthetic bacteria and eukaryotic cells. Chloroplasts have a small amount of DNA, similar to that of bacteria, and replicate themselves through a fission process. Chloroplast DNA is highly conserved. This means that it doesn't have a high rate of mutation or change. Inversions and other rearrangements are uncommon in flowering plant chloroplast DNA. Chloroplast DNA is not as highly repetitive as nuclear DNA. Chloroplast DNA is also useful for study because it is small compared to nuclear DNA. The chloroplast genome is about 134 kb in grasses (134,000 bases long).
Mitochondrial DNA is found in mitochondria only. Mitochondria also probably represent ancient symbiosis between respiratory bacteria and eukaryotic cells. Mitochondrial DNA is similar to chloroplast DNA in size and rate of change.
Polymerase Chain Reaction (PCR) Technology:
This process is used to increase amounts of DNA for further study. Very
small amounts of DNA can be turned into larger amounts for various types of
studies. DNA is extracted from the plant. It is heated to separate the two strands
of the double helix. The single-stranded DNA is cooled with materials necessary
for production of complementary strands. The enzyme DNA polymerase is added
together with all of the necessary bases and complimentary strands of DNA form
along both single strands of DNA at the same time. Once replication is complete,
the mixture is heated to separate the two strands of the new DNA, then the process
is repeated. Each heating/replication cycle doubles the number of copies of
the DNA segment.
Specific primers can be added to initiate replication at specific base sequences. The resulting double-stranded DNA fragments can be separated on electrophoretic gels where they migrate at rates according to their size.