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BIO505T Final Term Objective Guess Paper 2023

Essentials of Genetics (Theory) PDF 632 KBUpdated 23 Oct 2026
Final term past paper BIO505T Final Term Objective Guess Paper 2023 PDF 632 KB
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BIO505T Essentials of Genetics (Theory)
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BIO-301 MCQs FINAL TERM- 100% · GUESS PAPER 2023 · Essentials of Genetics · BY SULMAN ALI · OBJECTIVES

  •  Double mutation has a fitter phenotype than either single mutation.
  •  Proteins are made of "amino acids"
  •  Nucleotides contain "ribose sugar"
  •  Sequence of development “haploid cells diploid zygote"
  •  Diploid number is obtained after "fertilization"
  •  Colichine produces "polyploidy"
  •  The uses of vntr "geomic mapping etc"
  •  RNA is obtained from"cytoplasm"
  •  Northern blot is used for *RNA analysis*.
  •  The following is not chromosomal aberration is *mitosis*.
  •  R banding has dark bands of *adenine and thymine content*.
  •  Cancer and infertility are the result of *genetic mutations*.
  •  Colchicine is used to *promote polyploidy*.
  •  A cross for determination of the genotype of an individual is called a *test cross*.
  •  Autosomal dominant diseases are caused by *dominant alleles on autosomal
  • Mitochondrial DNA* is inherited through ovum, not sperm.
  •  Sequence difference compared to a reference standard present in at least 1-2% of a population is called *polymorphism*.
  •  Which on is sexual disease ____________________________Alzheimer's disease.
  • Discontinuous variations are entirely genetically controlled.
  •  forward genetics is defined as____ The identification of genes responsible for a specific phenotype without prior knowledge of the gene's function.
  •  genetic marker for a single locus is _______ RFLP, Microsatellite, STS.
  •  in x-linked recessive trait all are true except__ "In X-linked recessive traits, males

can be carriers of the trait."/ it is present in females more than males

 a healthy male and female have a sòn who is color blind .what is genetics of boy parents?

XcY

  •  Dark bands are those which contain fewer or less intense light waves, and light bands are those which contain more or more intense light waves.
  •  The chromosome number in an earthworm is 2.

likely genotypes of the boy's parents?

  • Boy = XaY (got recessive allele from mother) He will be color blind.
  •  Position depended method of disease identification following _______Reverse

genetics

  •  Molecular biology, forensic , genes mapping are application of ________________VNTR
  •  Groups of human chromosomes are __________________________7
  •  Dna precipitation k liye konsa chemical use hota?___Isopropanol
  •  Important reagents for pcr. Option mai sb hi mojood thy tu _____ALL
  •  Mitochondrial inheritance ki cgaracteristics di thi option mai. Ghalat konsi ye btana tha. These are present chose other than these (⚫ Heteroplasy ⚫ Variable expression ⚫ Pleiotropy ⚫ Reduced penetrance ⚫Functional somatic mosaic).
  • Q-PCR is commonly used to determine whether a DNA sequence is present in a sample and the number of its copies in the sample.
  •  Meiosis I ki characteristics pochi thi option mai. Ye b ALL
  •  In which pcr two pairs of primers are used.______Nested PCR
  •  In giemsa staining dark bands are rich in... A and T ans
  •  And light bands are rich in.... G and C ans
  •  During rna extraction, rna is extracted from the neucli of which cell. Rbc, wbc, or platelets
  • Erythrocytes k bry mak 1 mcqs tha______ Erythrocytes (red blood cells) do not contain nuclei. They neither synthesize nor contain RNA.
  •  Which fur color of rabbit have highest numbers of genotypes. Grey
  •  Which genetic disorder have lowest frequency. Ans autosomal recessive disorder
  •  Which is an autosomal recessive disorder? (⚫ Bloom syndrome ⚫ Carpenter

syndrome ⚫ Cystic fibrosis ⚫ Thalasemia ⚫Many forms of mental retardation)

  •  Which mutation shortens the protein? Ans non-sense mutation
  •  How many cases of turner syndrome are due to ring chromosome. Ans 20%
  •  During inversion what is reversed.___chromosome sequence/segments of
  •  Which mutation suppreses the effect of other mutation. Ans suppresion mutation
  • DOMINANT EPISTASIS: Epistatic gene exerts its affect with the presence of a dominant allele.
  •  Mutation that occur in regulatory region affects? Ans transcription, Translation

and splicing of protein

  • AUTOSOMAL DOMINANT DISEASES (⚫ Marfan syndrome ⚫ Huntington's disease ⚫ Retinoblastoma ⚫Waardenburg syndrome ⚫Myotonic dystrophy ⚫ Polycystic kidney disease ⚫ Achondroplasia ⚫ Polydactyly ⚫ Heredity hearing loss)
  • X-LINKED DOMINANT DISEASES: (⚫ Rett syndrome ⚫ Alport syndrome ⚫ Goltz syndrome ⚫ Fragile-X Syndrome)
  •  Homologous paired chromosomes have the same shape, size, and location of the centromere.
  •  in organic method of purification of DNA ...... IS USED TO remove protein (ans)

phenol chloroform

  •  ..... Is chelating agent(ans)EDTA
  •  ..... Result in two cells(ans) mitosis
  •  application thi VNTR ki uska answer bh VNTR hi th
  •  R banding has dark bands of: (ans) Heterochromatic
  •  Fur color in labrador retriever controlled by….(ans)2gene
  •  Two pairs of primer use in…(ans) nested PCR

probability that any son born will have pattern baldness?.. (ans)50%

  •  A mutation that are responsible for shorten of protein due to producing stop

codons….(ans)non sense mutation

  •  when allele of two gene segregate together and transmitted as a unit? What type of segregation occur... (Ans) Dependent segregation
  •  dna fingerprinting is an example of??VnTR
  •  If normal male and normal female are not color blind but their son is color blind what are the alleles of next generation: A) Son carry recessive allele
  •  Hemophilia is an example of____X linked chromosome.
  •  Two pairs of primer use in….. nested pcr
  •  Genes in drosophila.......13,700
  •  A mutation that are responsible for shorten of protein.......... Nonsense mutation
  •  ............. Caused frameshift mutation._______ Deletion
  •  First stage of mitosis.......Prophase
  •  First phase of mitosis........Prophase
  •  ............... is non-ionic buffer for DNA extraction ( cell lysis buffer)
  •  If both parents have heterozygous dominant disease, what will be the chance of a child not having that disease? (25%)
  •  microbiology, finger printing, genetic diversity and mapping of genomes are applications of........VNTR.
  •  Symbol of substitution ____ ">"
  •  RNA is genetic material in.....some viruses
  •  A type of genetic study in which , select a gene create a mutation then study its phenotype ............. Forward genetics.
  •  If two people who are both carrier for the genetically inherited fatal recessive disease decide to become parents , how many chances that their children will also be carriers.( 1

out of 4)

  •  Any change in nucleotide sequence of DNA gene is called......mutation
  •  Which disorder have the lowest frequency range.......X linked disorder.
  •  In phenol- chloroform DNA extraction lower organic phase contains........lipids
  •  DNA finger printing bioinformatics are applications of ( ans)VNTR
  •  R banding has dark bands of: ( ans) Heterochromatic
  •  Two pairs of primer use in…( ans) nested PCR
  •  A mutation that are responsible for shorten of protein due to producing stop codons….(
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