Write short notes on the following in about 150 words each : (a) Frame Shift mutation (10 marks) (b) Lampbrush chromosome and its significance (10 marks) (c) Reporter genes (10 marks) (d) Cell signalling and Cell receptors (10 marks) (e) DNA finger printing (10 marks)
हिंदी में पढ़ें
निम्नलिखित में से प्रत्येक पर लगभग 150 शब्दों में संक्षिप्त टिप्पणी लिखिए : (a) फ्रेमशिफ्ट उत्परिवर्तन (10 अंक) (b) लैम्पब्रुश गुणसूत्र तथा उसका महत्व (10 अंक) (c) रिपोर्टर जीन (10 अंक) (d) कोशिका संकेतन तथा कोशिका ग्राही (10 अंक) (e) डी एन ए फिंगर प्रिंटिंग (10 अंक)
Answer approach & key points
(a) A compact 150-word note defining frameshift mutation, explaining how insertion/deletion of a number of bases not a multiple of three shifts the reading frame, and stating its molecular consequences, causative mutagens and significance. 'Short note' means definition plus mechanism plus consequence plus an example, not an essay. (b) A 150-word note that must do two things explicitly asked: (i) describe the structure and occurrence of lampbrush chromosomes, and (ii) state their biological and cytogenetic significance. A labelled sketch of the chromomere-axis with paired lateral loops is expected. (c) A 150-word note defining reporter genes, listing the properties that make a gene a good reporter, naming the standard reporters with their gene symbols, sources, substrates and detection, and stating their applications in plant molecular biology. The distinction from selectable marker genes should be made. (d) A 150-word note covering both parts named in the question: (i) cell signalling as a perception-transduction-response sequence, and (ii) the classes of cell receptors, with named plant examples. Both halves must be present; an answer on signalling alone is incomplete. (e) A 150-word note on DNA fingerprinting: its basis in hypervariable repeat polymorphism, the classical Southern-blot/VNTR protocol and its modern PCR-STR successor, and its applications, with the plant/agricultural applications given due weight in a Botany paper.
- Definition: insertion or deletion of nucleotides not in multiples of three, shifting the reading frame
- Effect: altered codons downstream, premature stop, truncated non-functional protein; worked example
- Causes: acridine dyes (intercalation), polymerase slippage; named examples (CCR5-delta32, Tay-Sachs HEXA)
- Crick et al. 1961 T4 rII experiment proving the triplet code
- Occurrence: diplotene of meiotic prophase I in oocytes (amphibians, also birds, reptiles, insects); Flemming 1882, Rückert 1892
- Structure: bivalents with chiasmata, axis of chromomeres, paired lateral loops per chromatid with RNA-protein matrix
- Loops transcriptionally active; thin and thick ends
- Significance: stockpile of RNA for early embryo, model for transcription and RNA processing, gene mapping
- Definition: gene with easily assayed product used to monitor expression, promoter activity, transformation
- Properties: absent in host, sensitive quantitative assay, non-toxic, stable
- Examples with detection: lacZ, GUS, GFP, luciferase, CAT
- Uses (promoter analysis, protein localisation, screening) and difference from selectable markers
- Signalling steps: ligand, receptor, transduction, response, termination
- Types: endocrine, paracrine, autocrine, juxtacrine
- Transduction: second messengers (cAMP, Ca²⁺, IP3, DAG), phosphorylation cascades (MAPK)
- Receptors: cell-surface (GPCR, enzyme-linked, ion channel, plant RLKs) and intracellular (steroid, phytochrome, TIR1, GID1, PYR/PYL)
- Basis: hypervariable VNTR and STR repeats, individual-specific (Jeffreys 1984)
- Steps: DNA isolation, restriction digestion, electrophoresis, Southern blotting, probe hybridisation, autoradiography
- Modern STR-PCR with capillary electrophoresis
- Applications: forensics, paternity, disaster victims, wildlife, plant varieties; Indian pioneer Lalji Singh at CCMB