Molecular Basis Of Inheritance | Detailed One Shot | NEET 2024 | Dr. Gargi Singh

Unacademy NEET Toppers・2 minutes read

Dr. Gargi Singh is conducting a detailed series on genetics, focusing on DNA, RNA, transcription, and genes, crucial for exams. The session will cover topics like translation, human genome project, and DNA fingerprinting tomorrow, with the aim of providing a comprehensive understanding of genetics.

Insights

Dr. Gargi Singh conducts a detailed biology session beyond the NCERT syllabus, focusing on genetics and the molecular basis of inheritance.
The session aims to provide in-depth knowledge on DNA, RNA, transcription, and genes, with a significant emphasis on the structure and composition of nucleotides.
The discovery of DNA's double helix structure by Watson and Crick, based on X-ray Diffraction data from Franklin & Wilkins, revolutionized genetic understanding.
The importance of nucleotides, base pairing, and DNA replication mechanisms, including the semi-conservative nature demonstrated by Meselson and Stahl, are essential components of genetic studies.
The transcription process, involving promoters, terminators, and RNA polymerase, plays a crucial role in converting DNA into RNA for protein synthesis, highlighting the complexity of genetic regulation.

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Recent questions

What is the focus of Dr. Gargi's biology session?
Genetics
What is the primary genetic material?
DNA
What is the structure of DNA?
Double helix
What is the role of nucleotides in DNA?
Forming DNA sequences
What is the process of DNA replication?
Semi-conservative nature

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Summary

00:00

"Genetics Session with Dr. Gargi Singh"

The session is live on Unacademy NEET Toppers Channel with Dr. Gargi Singh, a biology expert.
Dr. Gargi is conducting a restart series covering biology topics, including those beyond NCERT syllabus.
The focus is on genetics, starting with the molecular basis of inheritance in two parts.
The chapter is crucial, with an expected 8-10 questions in exams, possibly increasing to 50 marks.
The session aims to provide a detailed understanding of DNA, RNA, transcription, and genes.
Tomorrow's session will cover translation, human genome project, DNA fingerprinting, and more.
Genetic material is primarily DNA, but RNA is also present, with exceptions.
Examples like Bacteriophage Pha 174 and Lam showcase varying nucleotide counts.
Human DNA contains 3.3*10^9 base pairs, crucial data for exams.
Detailed notes on nucleotide counts and base pairs are essential for understanding genetics.

15:59

"DNA Structure: Nucleotides, Bases, and Evolution"

DNA content discussed, focusing on structure and size
Nucleotides explained as comprising phosphate, sugar, and nitrogenous base
Sugar component of nucleotide identified as pentose with five carbons
Importance of numbering in DNA structure emphasized
Differentiation between DNA and RNA sugars clarified as deoxyribose and ribose, respectively
Nitrogenous bases categorized into purines and pyrimidines
Purines described as having two rings, while pyrimidines have one
Thymine highlighted as exclusive to DNA, while uracil is specific to RNA
Thymine's structure explained as a modification of uracil with a methyl group
Evolutionary significance of thymine in DNA stability due to genetic material requirements

33:13

Molecular Structures and Bonds in Nucleotides

Ene is a purine with two rings, one of six carbons and one of five carbons.
The structure of ene involves forming double bonds by alternating positions.
The structure of pyramiding involves a ring with nitrogen and oxygen atoms in alternate positions.
Nucleotides are formed by combining nitrogenous bases, sugars, and phosphates.
The bond between sugar and nitrogenous bases is called glycosidic.
Phosphate forms a bond with sugar in nucleotides, known as a phosphoester bond.
Nucleotides can form phosphodiester bonds when binding with other nucleotides.
Nucleosides are formed by combining nitrogenous bases and sugars.
Nucleotides are formed by adding phosphates to nucleosides.
The structure of DNA is a double helix, discovered by Watson and Crick in 1953.

50:12

"DNA Structure and Replication: Key Discoveries"

The X-ray Diffraction data provided by Franklin & Wilkins was crucial for the study.
The data was used to propose the Double Helix Model for the Structure of DNA in 1953 by Watson and Crick.
The proposition was based on the observation of Erwin Schar Gough regarding base pairing in DNA.
Shar Gaff's rule states that the ratio between Adenine and Thymine, and Guanine and Cytosine, is constant and equal.
The Shargh rule emphasizes that the amount of Purine equals the amount of Pyrimidine in DNA.
The structure of DNA involves nucleotides made of sugar, phosphate, and nitrogen bases.
Nucleotides form poly nucleotide chains connected by hydrogen bonds through base pairing.
The fifth position in a nucleotide determines the base pairing with Adenine or Thymine.
The concept of DNA replication involves nucleotides attacking the phosphate group at the third position.
The process of DNA replication requires the three prime phosphate group for attachment.

01:08:54

"DNA Replication: Primers, Bonds, Helix Structure"

DNA replication involves the use of primers, which are small segments near DNA that are related to RNA.
Primers are necessary because DNA synthesis cannot start on its own.
The O group in the third position is crucial for DNA repair during replication.
Phospho-ester bonds are formed between nucleotides, held together by phosphate groups.
DNA synthesis occurs in a specific direction, with the fifth position attacking the third position.
The orientation of DNA chains is anti-parallel, with the five prime and three prime ends connecting.
Hydrogen bonds are formed between nitrogen bases to connect the DNA chains.
The diameter of DNA is 20 angstroms, with 10 base pairs in one turn.
The pitch of DNA, representing one turn, is 3.4 nanometers with 10 base pairs.
DNA forms a double helix structure with coils, held together by hydrogen bonds and base pairings.

01:26:18

DNA Structure and Function Explained

The distance between two base pairs in DNA is 0.34 nanometers.
Phosphate at the end of the five prime end of DNA forms a bond with sugar.
The structure of DNA involves phosphate on the five prime end bonding with sugar on the three prime end.
The distance between poly nucleotide chains in DNA remains constant due to base pairing.
Nucleotides form base pairs, with one nucleotide pairing with another.
The pitch of DNA involves a complete rotation after 3.4 nanometers.
Reverse transcription involves RNA being formed from DNA, known as transcription.
Reverse transcription, also called tameism, involves DNA being formed from RNA.
The length of DNA in human cells is 6.6 * 10^9 base pairs.
DNA packaging involves DNA being negatively charged and wrapped around histone proteins.

01:46:00

"DNA, Nucleosomes, and Chromatin Structure Explained"

Eight units have been installed, with four visible behind and four in front.
DNA is wrapped around the units to form histone proteins.
The histone proteins are coiled with DNA to create nucleosomes.
Each nucleosome contains 200 base pairs of DNA.
A1 histone is not part of the nucleosome structure.
The appearance of nucleosomes resembles a string of pearls.
Chromatin can be either euchromatin (loosely packed) or heterochromatin (densely packed).
Transcriptional activity is linked to chromatin structure.
Genetic material was identified as DNA through the Griffith experiment in 1928.
Transformation occurs when DNA from one strain is taken up by another, changing its characteristics.

02:03:30

"DNA Proven Genetic Material Through Experiments"

The transforming principle is a genetic material, but its nature as DNA, RNA, or protein is unknown.
Griffith's data was stolen, leading to further experiments to determine the biochemical nature of the transforming principle.
Avery, McCall, and McCarty established that DNA is the genetic material based on Griffith's experiment.
Different enzymes are used to isolate DNA, RNA, and protein, proving DNA's role in transformation.
Hershey and Chase provided unequivocal proof that DNA is the genetic material through radioactivity experiments.
The experiment involved infecting bacteria with a virus to show DNA's entry and protein's exclusion from the bacteria.
The experiment confirmed DNA as the genetic material by detecting radioactivity in bacteria with DNA but not protein.
Genetic material should be stable, non-reactive, and exhibit Mendelian characters like DNA.
RNA and DNA differ in ribose sugar structure, with RNA being more reactive and prone to mutation.
The RNA world theory suggests RNA's role in protein synthesis with higher regulation and stability compared to DNA.

02:21:32

"DNA Stability, Replication, and Pairing Mechanisms Discussed"

Thyme DNA provides more stability, discussed in a structured talk with children watching.
Theoretical question posed about the number of true seeds in nucleosomes, answered as 30 million.
Differentiation between DNA and DNA enzyme explained, emphasizing DNA's role in breaking down DNA.
Discussion on DNA and RNA World, highlighting RNA's catalytic properties.
Specific pairing mechanisms for genetic material proposed by Watson and Crick.
Proposal for DNA replication mechanism involving two separate strands acting as templates for new complementary strands.
Detailed explanation of DNA replication process, emphasizing the creation of new DNA sequences.
Experimental proof of DNA replication's semi-conservative nature provided by Meselson and Stahl in 1958.
Experimental method using heavy and light isotopes to demonstrate DNA replication.
Detailed walkthrough of an experiment demonstrating DNA replication using heavy and light isotopes, showcasing the hybridization process.

02:40:17

"Teaching Challenges and DNA Synthesis Process"

The speaker discusses the challenges of teaching for long hours, emphasizing the need for motivation and energy.
Teaching sessions drain the speaker's energy, making it difficult to maintain a frequent schedule.
The speaker reflects on the importance of timing and seizing opportunities in the teaching profession.
The discussion shifts to DNA rape case analysis, highlighting the process of DNA synthesis.
To create DNA, nucleotides, energy, primer, DNA polymerase, magnesium ion, helicase, and isomerases are essential.
The speaker explains the role of single-strand binding proteins in DNA synthesis.
Energy for DNA synthesis is obtained through breaking high-energy phosphate bonds in nucleotides like deoxy adenosine triphosphate (DATP).
The importance of primer in DNA synthesis is emphasized for forming bonds at the third position of nucleotides.
The need for helicase to separate DNA strands and topoisomerase to release supercoiling for DNA synthesis is discussed.
The speaker demonstrates the process of unwinding DNA strands to prevent supercoiling and ensure successful DNA synthesis.

03:01:48

Forbidden Love: DNA Replication and Transcription

The story involves a boy and a girl whose families disapprove of their relationship.
The families separate the boy and girl, represented as two strands.
Single-stranded binding proteins are used to prevent the boy and girl from meeting.
The girl's brother, acting as an uncle, is responsible for keeping them apart.
Topo isomerase uncle helps in removing the tension caused by the separation.
DNA replication involves DNA polymerase creating new strands from nucleotides.
DNA replication occurs at specific points called origin of replication.
Replication results in the formation of Okazaki fragments.
Okazaki fragments are later joined together with the help of DNA ligase.
Transcription involves converting DNA into RNA, with only one DNA strand acting as a template.

03:19:04

RNA Transcription: Promoter to Termination Process

Connecting RNA molecules with different sequences can lead to complications in protein synthesis, potentially resulting in the coding for two different proteins from one DNA segment.
Two RNA molecules producing complementary sequences can form double-stranded RNA, preventing translation and protein synthesis.
Understanding the roles of promoters, structural genes, and terminators in the transcription process is crucial for proper RNA synthesis.
Promoters initiate transcription by helping RNA polymerase bind to the DNA template, while terminators stop the process.
Specific sequences like the Tata Box are essential for RNA polymerase to attach to the promoter and initiate transcription.
RNA polymerase consists of a core enzyme and a sigma factor, with the sigma factor crucial for binding to the promoter and starting transcription.
Transcription involves unwinding DNA, adding ribonucleotides to form RNA, and eventually terminating the process with the help of the Rho factor.
The Rho factor binds to RNA polymerase at the terminator, halting transcription and completing the RNA synthesis process.
The transcription process involves multiple steps, including initiation, elongation with ribonucleotide addition, and termination with the Rho factor's intervention.
Understanding the intricate process of transcription, from promoter binding to termination, is essential for successful RNA synthesis and protein production.

03:38:54

"Session schedule and breaks for children"

The session will end, and the next session is tomorrow at 10 am. The chapter will be completed this week, and comments are encouraged for motivation.
Children are advised to take a 15-minute break, have lunch, and drink water before the next session, emphasizing the importance of rest and hydration.

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