The major research advances that led to our modern understanding of DNA were investigated in the 1920s - 1950s.
The genetic material, DNA or proteins, was investigated in the 1920s - 1950s.
Griffith (1928) discovered that genetic traits can be transferred between cells, using an unknown substance from virulent bacteria to transform harmless bacteria.
Avery, MacLeod, & McCarty (1944) demonstrated that DNA is the transforming substance, by sequentially inactivating RNA, protein, and DNA.
Nucleotide structure, consisting of a 5 carbon sugar, a phosphate group, and a nitrogenous base, was known since the 1920s.
Chargaff’s (1950) Rule states that the number of A=T and the number of C=G are constant in DNA.
Rosalind Franklin (1953) discovered that DNA is shaped like a helix (corkscrew) and has a consistent diameter.
Watson & Crick (1953), based on Franklin’s work, proposed that DNA is a double helix with a sugar-phosphate backbone on the outside.
Watson & Crick (1953) stated that the two strands of DNA are held together by hydrogen bonds between complementary base-pairs.
Watson & Crick (1953) stated that the two stands of DNA are antiparallel, running in opposite directions 5’-3’.
DNA synthesis, where DNA is synthesized in the 5’- > 3’ direction only, is a key aspect of DNA replication.
DNA replication involves a replication fork, a Y-shaped region where parental strands are unwound.
RNA (ribonucleic acid) contains ribose, contains uracil (U), is usually single-stranded, is shorter than DNA, and is temporary.
DNA (deoxyribonucleic acid) contains deoxyribose, contains thymine (T), is usually double-stranded, is longer than RNA, and is permanent.
Transcription (Gene expression) involves converting the information in DNA into a protein.
A is the same, why do your blood cells look and act different than your skin cells? Different cells express different proteins. This is called differential gene expression.
RNA polymerase synthesizes a strand of mRNA in the 5’ to 3’ direction, transcription begins at a promoter sequence and ends at a terminator sequence.
The process of splicing involves a complex of snRNA and proteins, the spliceosome, which forms a lariat, cuts mRNA, and joins exons.
In prokaryotes, the entire process of gene expression occurs in the cytoplasm, translation begins before transcription ends, and one mRNA may contain multiple genes (operon).
Splicing: removes introns (noncoding segments) and joins exons (coding segments).
Transcription: Synthesis of mRNA from DNA.
5’ Cap: Methylated GTP added “backwards” to 5’ end of pre-mRNA, protects from degradation, helps translation initiation.
In eukaryotes, transcription occurs in the nucleus, RNA is processed before leaving the nucleus, and translation occurs in the cytoplasm.