
Learn how the genetic alphabet A, G, C, T encodes genomes with two-bit logic, comparing prokaryote and human genomes through books as an information analogy.
Zoom in on metaphase chromosomes, showing rosettes and solenoids within a 30-nm fiber, with histone octamers and h1 forming chromatosomes—beads-on-a-string dna packaging revealed by light to x-ray methods.
Examine nucleotides as the building blocks of DNA and RNA, detailing purines and pyrimidines, N-glycosidic bonds to ribose or deoxyribose, phosphate linkages, and mono-, di-, and tri-phosphates.
Nucleotides act as enzyme activators and coenzymes in metabolism, energy currencies like ATP and GDP, activated intermediates with UDP, CDP, and SAM, and the building blocks of RNA and DNA.
Explore the architecture of polynucleotides: nucleotide structure, energy-storing phosphate bonds, phosphodiester linkages, DNA and RNA forms, Chargaff base pairing, and 3' to 5' polarity.
Explore the four-letter genetic alphabet and base pairing, the B, A, and Z DNA forms with major and minor grooves, and how pH and temperature affect denaturation.
Explore the diverse roles of RNA, including mRNA, tRNA, and rRNA, their structures, processing, and translation into proteins, plus RNA interference by miRNA and siRNA.
Follow the flow of genetic information from DNA to RNA to protein under the central dogma. Review key experiments establishing DNA as the genetic material and outlining replication, transcription, translation.
Explore prokaryotes as model organisms, focusing on bacteria and E. coli, their cell structure, plasmids and episomes, transposons, and horizontal gene transfer.
Describe the eukaryotic cell cycle from interphase (G1, S, G2, sometimes G0) to mitosis and cytokinesis, detailing chromatin changes, kinetochores, spindle dynamics, and telomere regulation.
Trace how external regulators engage receptors, activate MAPK signaling, and drive cyclin–CDK complexes to regulate E2F release, the G1 to S transition, DNA replication, MPF activity, G1/G2/M checkpoints, and apoptosis.
Explore how persistent cellular stress leads to mutations in cell-cycle genes, triggering dysplasia, metaplasia, neoplasia, and eventually invasive, metastatic cancer.
Proto-oncogenes promote cell growth but mutate into oncogenes, as with ras and myc, triggering cyclins and CDKs; tumor suppressors like p53, p16, ARF restrain growth to prevent cancer.
Explore the oldest texts and scripts, from pictographs to cuneiform and beyond, and connect this quest to life’s molecular history—from an RNA–protein world to DNA, the oldest living scroll.
Explain replication prerequisites and the duplication machinery, including consensus sequence recognition by Dna A protein, strand separation, antiparallel reading 3'→5' and synthesis 5'→3', plus helicase, primase, polymerase I–III, ligase, Tus.
Identify how the prokaryotic origin of replication is recognized at an AT-rich consensus sequence, where DNAa and helicases melt DNA to form replication bubbles and forks.
Explore why DNA replication is semi discontinuous, with continuous leading strand synthesis and fragmentary lagging strand synthesis via primers, Okazaki fragments, and ligation.
Describe elongation in prokaryotes, including primase and the primosome, RNA primers, and DNA polymerases I and III. Explain primer removal, replacement, and ligase sealing during leading and lagging strand synthesis.
The primosome initiates primers on the leading and lagging strands, while Polymerase III extends them. Polymerase I removes primers and fills with deoxyribonucleotides using proofreading and exonuclease activities.
Explains how the lagging strand is synthesized in fragments (Okazaki fragments), detailing the roles of primase, polymerase III, polymerase I, and ligase in primer removal, nick sealing, and fragment joining.
Prokaryotic replication terminates when two forks meet ter sites bound by tus proteins, forming tus-ter complexes that block or allow passage, ultimately separating the two circular chromosomes.
Genetics and molecular biology for medical students explores how DNA is copied with strict proofreading, base pairing rules, and directional synthesis, then repaired by surveyor proteins before cell division.
This course is basically designed for medical students; however, it is also an invaluable resource for students of other health related disciplines like biotechnology, pharmacy, nursing, biophysics, bio-engineering, bioinformatics and dentistry. In addition to the well-illustrated video lectures, the core concepts are reinforced with quick review sheets and end of lecture quizzes.
In addition to detailed explanation of the structure and functions of nucleotides and nucleic acids, Dr Fatahiya Kashif explains how the linear DNA in a human cell is packaged in a highly organized and compact manner within the 23 pairs of chromosomes without being entangled. There is special segments on prokaryotes as our model organisms and stages of the eukaryotic cell cycle.
Keeping in view, the volatile nature of this subject, and the fact, that medical students are already confronted with an overwhelming volume of medical terminology; the most challenging concepts are presented in a simple and palatable format using animations and mnemonics. Furthermore, each section emphasizes the medical relevance of biochemistry with clinical and research applications. The course is continuously being updated with additional lectures and resources.