DNA replication is the process by which DNA duplicates itself for cell division. It involves unwinding of the DNA double helix, formation of a replication fork, and synthesis of new complementary strands. Each original DNA strand acts as a template for new strand synthesis by DNA polymerase in the 5' to 3' direction. RNA primers are required for initiation, and Okazaki fragments are produced on the lagging strand. Replication proceeds bidirectionally from an origin of replication site and involves multiple enzymes until the replication fork meets, at which point termination occurs. Differences between prokaryotic and eukaryotic replication include RNA primer length, number of DNA polymerases, and presence of histones and telomeres in eukaryotes
Introduction
History
Definition
Classification of DNA Polymerase
Mechanism of DNA Replication
Process of DNA Replication
Initiation
Regulation
Termination
Conclusion
Reference
DNA replication is semi-conservative, one strand serves as the template for the second strand. Furthermore, DNA replication only occurs at a specific step in the cell cycle.
DNA replication in eukaryotes is much more complicated than in prokaryotes, although there are many similar aspects.
DNA replication is a biological process that occurs in all living organisms and copies their DNA; it is the basis for biological inheritance.
Eukaryotic cells can only initiate DNA replication at a specific point in the cell cycle, the beginning of S phase.
Due to the size of chromosomes in eukaryotes, eukaryotic chromosomes contain multiple origins of replication
Replication Introduction , DNA replicating Models , Meselson and Stahl Experiments , Circuler Model of DNA replication , Replication in Prokaryotes , Replication In Eukaryotes , Comparison Between Prokaryotes and Eukaryotes Replicaton and PCR (Polymerease Chain Reaction)
Prokaryotic DNA replication : These slides contains basics of the prokaryotic DNA replication for S.Y.B.Sc and T.Y.B.Sc students of Microbiology and biotechnology
It covers topics like Enzymes used in replication, Semiconservative replication, Meselson and Stahl experiment, Termination of replication, modes of replication: theta and rolling circle, basic rules of replication
Introduction
History
Definition
Classification of DNA Polymerase
Mechanism of DNA Replication
Process of DNA Replication
Initiation
Regulation
Termination
Conclusion
Reference
DNA replication is semi-conservative, one strand serves as the template for the second strand. Furthermore, DNA replication only occurs at a specific step in the cell cycle.
DNA replication in eukaryotes is much more complicated than in prokaryotes, although there are many similar aspects.
DNA replication is a biological process that occurs in all living organisms and copies their DNA; it is the basis for biological inheritance.
Eukaryotic cells can only initiate DNA replication at a specific point in the cell cycle, the beginning of S phase.
Due to the size of chromosomes in eukaryotes, eukaryotic chromosomes contain multiple origins of replication
Replication Introduction , DNA replicating Models , Meselson and Stahl Experiments , Circuler Model of DNA replication , Replication in Prokaryotes , Replication In Eukaryotes , Comparison Between Prokaryotes and Eukaryotes Replicaton and PCR (Polymerease Chain Reaction)
Prokaryotic DNA replication : These slides contains basics of the prokaryotic DNA replication for S.Y.B.Sc and T.Y.B.Sc students of Microbiology and biotechnology
It covers topics like Enzymes used in replication, Semiconservative replication, Meselson and Stahl experiment, Termination of replication, modes of replication: theta and rolling circle, basic rules of replication
This presentation is targeted for MBBS, MD and BDS students that describes briefly about aetiopathogenesis, tumour markers, anti cancer agents, apoptosis
Glycine is an aliphatic amino acid which gives rise to many vital derivatives. This is a non-essential amino acid. This presentation is targeted for MBBS, MD, BDS and general Biochemistry students.
it is about how ammonia is detoxified to urea and its biomedical significance. This PPT can be used by students of MBBS, MD, BDS and general Biochemistry students
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
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Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
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Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
3. CENTRAL DOGMA
The Flow of Information: DNA → RNA → Protein
A gene is expressed in two steps:
DNA is transcribed to RNA
Then RNA is translated into protein
4. DNA- major store of genetic
information
To transfer genetic information from
parent to daughter cell, DNA must be
duplicated.
DNA duplication– DNA
REPLICATION
DNA→DNA
Semi- conservative replication
7. Salient features of replication
Each strand serves as a template/mould,
over which a new complementary strand is
synthesized
Base-pairing rule is maintained
Polymerization from 5’-3’ direction
Old DNA is not degraded but conserved
DNA polymerase synthesises a new
complementary strand
9. Steps of DNA replication
Identification of origin of replication
Unwinding of dsDNA to provide an ssDNA
template
Formation of replication fork
Initiation of DNA synthesis and elongation
Formation of replication bubbles with
ligation of the newly synthesised DNA
segments
Reconstitution of chromatin structure
10. 3 stages of replication
Initiation
Elongation
Termination
11. Initiation
Replication starts with recognition of ori
(origin of replication)
Single site of ori– bacteria
Multiple sites– mammals
dnaA protein binds to ori
↓
Local denaturation & unwinding of an
adjacent A-T rich region
12.
13. dnaB / Helicase– Binds to ori and unwinds
& separates the strands using ATP
↓
Replication fork formed
Topoisomerases– Relieve supercoils
Type I– Breaks one strand of DNA
Type II– Breaks both strands
Introduces negative supercoils
SSB (Single strand binding protein)-
Stabilizes the separated strands and
prevents reannealing.
14. Mammals- SSB counterpart is RFA
(replication factor)
dnaC protein– reqd. for dnaB binding
at ori
dnaG / Primase– Complexes with
proteins to form PRIMOSOME
↓
RNA primer synthesis
16. RNA primer
10-200 nucleotides long
Primase in prokaryotes
DNAP α- eukaryotes
Nucleophilic attack by 3’- OH group of the
RNA primer on the phosphate of the first
entering deoxynucleotide triphosphate
20. Elongation
After RNA primers laid down, 2 DNA
polymerase III complexes attach
Leading strand & lagging strand
DNA chain which runs in 3’-5’ direction
copied by DNAP III in 5’-3’ direction in a
continuous manner
Okazaki fragments on lagging strand
DNAP I– removes RNA primers and fills in
the gap between okazaki fragments
Ligase– joins the segments
21.
22. Okazaki fragments
Short stretches of 150-250bp (eukaryotes)
Found on lagging strand during DNA
replication
Later gap is filled by DNAP I and joined by
DNA ligase enzymes
Found in both eukaryotes and prokaryotes
Approx. 250 per replication fork
24. Properties of DNAP
Chain elongation– 100
nucleotides/sec in mammals
Proof reading-- rectification
Processivity– How many nucleotides
are to be added before it dislodges
27. ter binding protein – binds to the sequence
↓
prevents helicase from
further action
↓
termination of replication
28. Which factor triggers DNA
replication???
External signals are delivered to cells
during the G1 phase of the cell cycle and
activate the synthesis of cyclins
Cyclins form complexes with cyclin-
dependent kinases (CDK)
Cascade of reaction
Synthesis of S phase proteins like DNAP
and thymidylate synthase
29. Eukaryotic replication
Binding of origin recognition complex(ORC)
to origins of replication during G1 phase
↓
ORC serves as a platform for highly
complicated pre-RC complex formation
↓
Converted to RC by CDK and Dbf4-
dependent kinase
↓
DNA polymerase α- primase
complex synthesizes first primer
30. 2 characteristic features
Histone complexes
Telomeres- repeated end sequences of
(TTAGGG)n and have typical sizes of 15–20 kb
at birth
↓
In somatic cells it is shortened after each cycle
↓
Germline and cancer cells have telomerases
↓
extend the 5′ end of lagging strands
32. Modification after replication
Methylation of DNA
At C5 of C
Catalysed by DNA methyl transferase
Methylation occurs at G-C rich region of
promoter sequence
>90% methyl C s are in CpG dinucleotides
Methylated areas- transcriptionally silent
Aberrant methylation- cancer, ageing, ROS
dependent damage
33. Difference between prokaryotic and eukaryotic
replication
Features Prokaryotes Eukaryotes
RNA primer
length
~50 nucleotides 9 nucleotides
DNAP 3; I,II,III 5; α,β,γ,ε,δ
Number of
origin
Single Many
Okazaki
fragments
1000-2000
nucleotides
~250
nucleotides
Rate of
replication
~500
nucleotides/sec
~100
nucleotides/sec
34. DNA replicates once and once only
Pre-replicative sequence is formed-
ORC-DNA complex with Cdc6 and Cdt1 at
G1-S phase
New nucleosomes are assembled behind
the replication fork
35. Inhibitors of DNA replication
Topoisomerase II (DNA gyrase) inhibitor
Novobiocin– prevents ATP binding to gyrase
Nalidixic acid & Ciprofloxacin- interfere with the
breakage and rejoining of DNA chains
Camptothecin– inhibits human topoisomerase I
Nucleotide analogues– 2,3 dioxyinosine,
Cytarabine
Zidovudine, Acyclovir- terminate DNA chain
elongation
36. Be like the stem cell-differentiate yourself
from others