PSC Biology Questions

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    PSC Biology Questions. We covered all the PSC Biology Questions in this post for free so that you can practice well for the exam.

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    PSC Biology Questions for Students

    Quick Quiz

    Which of the following is a function of sphincter muscles?

    (a) Control peristalsis.

    (b) Grind large food particles.

    (c) Secrete digestive juices into the GI tract.

    (d) Control the passage of food through the GI tract.

    Option d – Control the passage of food through the GI tract

    Which one among the following statements is not correct?

    (a) Pulses are rich in proteins.

    (b) Milk is a rich source of Vitamin A.

    (c) Cereals are a very poor source of carbohydrates.

    (d) Vegetables are a rich source of minerals.

    Option c – Cereals are a very poor source of carbohydrates

    In the human digestive system, the process of digestion starts in

    (a) Esophagus

    (b) Buccal cavity

    (c) Duodenum

    (d) Stomach

    Option b – Buccal cavity

    The action of pepsin is to

    (a) Curdle milk.

    (b) Break down proteins to peptones.

    (c) Break down polypeptides into amino acids.

    (d) Break down polysaccharides into disaccharides.

    Option b – Break down proteins to peptones

    The main factor of evolution is

    (a) Mutation

    (b) Achieved quality

    (c) Vaginal birth

    (d) Natural selection

    Option d – Natural selection

    Which of the following situations would most likely result in the highest rate of natural selection?

    (a) Reproduction by asexual method

    (b) Low mutation in a stable environment

    (c) Little competition

    (d) Reproduction by sexual method

    Option d – Reproduction by sexual method

    Genetic drift operates in

    (a) large isolated populations

    (b) small isolated populations

    (c) fast reproductive populations

    (d) slow reproductive populations

    Option b – small isolated populations

    The biological species concept of organisms is based on

    (a) morphological traits

    (b) evolutionary traits

    (c) reproductive isolation

    (d) geographical isolation

    Option c – reproductive isolation

    Living organisms are kept separate from closely related species inhabiting the same geographical region by a reproductive isolating mechanism called

    (a) phylogenetic species concept

    (b) morphological species concept

    (c) genetic species concept

    (d) biological species concept

    Option d – biological species concept

    The biological concept of species is mainly based on

    (a) reproductive isolation

    (b) morphological features only

    (c) method of reproduction only

    (d) morphology and method of reproduction

    Option d – morphology and method of reproduction

    Among the following, which one is not an ape?

    (a) Gibbon

    (b) Urangutan

    (c) Gorilla

    (d) Langur

    Option d – Langur

    The difference between Homo sapiens and Homo erectus was

    (a) Homo sapiens originated in Africa, while Homo erectus originated in Asia.

    (b) Homo erectus were much smaller in size than Homo sapiens.

    (c) Homo erectus stayed in Africa, while Homo sapiens did not.

    (d) The size of the brain of Homo erectus was smaller than that of Homo sapiens.

    Option d – The size of the brain of Homo erectus was smaller than that of Homo sapiens

    Homo erectus evolved about 1.7 million years ago. They used fire and tools and also used animal hides as clothing. The fossil of Homo erectus was named as

    (a) Neanderthal man

    (b) Cro-magnon man

    (c) Java ape man

    (d) Proconsul

    Option c – Java ape man

    Anthropoids evolved into

    (a) apes, proconsul, and monkeys

    (b) apes, Cro-magnon men, and old-world monkeys

    (c) Proconsul, New World Monkeys, and Peking man

    (d) new world monkeys, proconsul, and Homo habilis

    Option a – apes, proconsul, and monkeys

    Mammoth is the ancestor of

    (a) dog

    (b) horse

    (c) camel

    (d) elephant

    Option d – elephant

    The latest ancestor of modern humans is

    (a) Java man

    (b) Cro-Magnon man

    (c) Neanderthal man

    (d) Peking man

    Option b – Cro-Magnon man

    Double-helical structure of DNA was given by

    (a) Jacob and Monod

    (b) Watson and Crick

    (c) H G Khorana

    (d) None of the above

    Option b – Watson and Crick

    Mendel selected pea plants for his experiment because

    (a) they are cheaper

    (b) they are easily available

    (c) they are of great economic importance

    (d) they have contrasting traits

    Option d – they have contrasting traits

    Who is the father of modern genetics?

    (a) Gregor Johann Mendel

    (b) Hugo De Vries

    (c) Charles Darwin

    (d) Thomas Hunt Morgan

    Option a – Gregor Johann Mendel

    Mendel worked on

    (a) edible pea

    (b) wild pea

    (c) garden pea

    (d) pigeon pea

    Option c – garden pea

    Gregor Johann Mendel is famous for

    (a) Cell Theory

    (b) Mutation Principle

    (c) Law of Heredity

    (d) Heredity of acquired characters

    Option c – Law of Heredity

    The unit of heredity in our body is called

    (a) Chromosome

    (b) DNA

    (c) Gene

    (d) Nucleus

    Option c – Gene

    Which of the following is responsible for controlling the hereditary characteristics of living cells?

    (a) Enzyme

    (b) Hormone

    (c) RNA

    (d) DNA

    Option d – DNA

    Linkage was first suggested by

    (a) Sutton and Boveri

    (b) Morgan

    (c) de Vries

    (d) Pasteur

    Option b – Morgan

    Linked genes are present on

    (a) the same chromosome

    (b) different chromosomes

    (c) heterologous chromosomes

    (d) paired chromosomes

    Option a – the same chromosome

    Mendel’s principles of inheritance are based on

    (a) vegetative reproduction

    (b) asexual reproduction

    (c) sexual reproduction

    (d) All of the above

    Option c – sexual reproduction

    Jumping genes, transposons, or movable genetic elements were discovered by Barbara McClintock in

    (a) maize

    (b) wheat

    (c) barley

    (d) rice

    Option a – maize

    Who is responsible for the sex determination of a child?

    (a) Father

    (b) Mother

    (c) Both (a) and (b)

    (d) None of the above

    Option a – Father

    Chromosomes can be counted best in

    (a) Metaphase

    (b) Early prophase

    (c) Mid prophase

    (d) Late prophase

    Option a – Metaphase

    An increase in age decreases

    (a) crossing over

    (b) linkage

    (c) polyploidy

    (d) mutations

    Option a – crossing over

    Genes present on Y-chromosomes are called

    (a) holandric genes

    (b) basic genes

    (c) pleiotropic genes

    (d) polygenic genes

    Option a – holandric genes

    Sex determination by environmental factors is commonly observed in

    (a) Drosophila melanogaster

    (b) Mirabilis jalapa

    (c) Melandrium album

    (d) Bonellia Viridis

    Option d – Bonellia Viridis

    By which combination of chromosomes will a child be male?

    (a) X from male and X from female

    (b) X from male and Y from female

    (c) Y from male and X from female

    (d) Y from male and Y from female

    Option c – Y from male and X from female

    The strength of the linkage between two genes is

    (a) proportionate to the distance between them

    (b) inversely proportionate to the distance between them

    (c) dependent on the chromosomes

    (d) dependent on the size of chromosomes

    Option b – inversely proportionate to the distance between them

    Linkage and crossing over are

    (a) the same phenomena

    (b) different phenomena

    (c) opposite phenomena

    (d) identical phenomena

    Option c – opposite phenomena

    Genes are made up of

    (a) nucleic acids

    (b) proteins

    (c) carbohydrates

    (d) lipids

    Option a – nucleic acids

    The cancer-causing gene is

    (a) protooncogene

    (b) oncogene

    (c) transposon

    (d) mutable gene

    Option b – oncogene

    Who among the following was awarded the Nobel Prize for the artificial synthesis of nucleic acids?

    (a) Ochoa, Kornberg, and HG Khorana

    (b) Jacob and Monod

    (c) Gierer and Schwann

    (d) Hershey and Aunt Julia

    Option a – Ochoa, Kornberg, and HG Khorana

    Change in the basic sequence of a gene is known as

    (a) mutation

    (b) transversion

    (c) conjugation

    (d) reproduction

    Option a – mutation

    Which phenomenon leads to the variation in DNA?

    (a) DNA Mutation

    (b) Linkage

    (c) Both (a) and (b)

    (d) Mitosis

    Option a – DNA Mutation

    Chromosomal aberrations are commonly found in

    (a) cancer cells

    (b) normal cells

    (c) healthy cells

    (d) autosomal cells

    Option a – cancer cells

    Point mutation arises due to a change in

    (a) a single base of DNA

    (b) a single base pair of DNA

    (c) a segment of DNA

    (d) a double base pair of DNA

    Option a – a single base of DNA

    A classical example of point mutation is

    (a) sickle-cell anemia

    (b) thalassemia

    (c) cancer

    (d) All of the above

    Option a – sickle-cell anemia

    Frameshift mutation arises due to

    (a) deletion of a base pair of DNA

    (b) insertion of a base pair of DNA

    (c) Both (a) and (b)

    (d) change in a single base pair of DNA

    Option c – Both (a) and (b)

    Mutagens are

    (a) chemical agents that cause changes in DNA

    (b) physical agents that cause mutations

    (c) cancer-producing agents

    (d) Both (a) and (b)

    Option d – Both (a) and (b)

    Genes located on mitochondrial DNA

    (a) generally show maternal inheritance

    (b) are always inherited from the male parent

    (c) show biparental inheritance

    (d) are not inherited like nuclear genes

    Option a – generally show maternal inheritance

    The number of chromosomes in a normal human body cell is

    (a) 43

    (b) 44

    (c) 45

    (d) 46

    Option d – 46

    Sexual reproduction causes genetic variation because of

    (a) blending of genes

    (b) chromosomal changes

    (c) shuffling of genes

    (d) All of the above

    Option d – All of the above

    Mutation is a phenomenon that results in the alteration of

    (a) sequence

    (b) carbohydrates

    (c) proteins

    (d) fat

    Option a – sequence

    Mutation may result in

    (a) a change in genotype

    (b) a change in phenotype

    (c) a change in metabolism

    (d) All of the above

    Option d – All of the above

    For a colorblind person, the red color appears as

    (a) yellow

    (b) blue

    (c) green

    (d) violet

    Option c – green

    Barr body is absent in somatic cells of

    (a) Klinefelter syndrome individual.

    (b) Triple X syndrome individual.

    (c) Turner syndrome individual.

    (d) Sub-human mammalian female individual.

    Option c – Turner syndrome individual

    Which of the following is an X-linked genetic disease?

    (a) Becker’s muscular dystrophy

    (b) Daltonism Color Blindness

    (c) Martin-Bell syndrome

    (d) All of the above

    Option d – All of the above

    Down’s syndrome is due to

    (a) chromosome number increase in the 21st pair autosome.

    (b) chromosome number decreases in the 21st pair autosome.

    (c) chromosome number increases in the 18th pair autosome.

    (d) chromosome number decreases in the 18th pair autosome.

    Option a – chromosome number increase in the 21st pair autosome

    Gynandromorph is

    (a) male with female traits.

    (b) female with male traits.

    (c) half male and half female.

    (d) None of the above

    Option c – half male and half female

    Which one of the following is not a genetic disorder?

    (a) Color blindness

    (b) Down’s syndrome

    (c) Hemophilia

    (d) Xerophthalmia

    Option d – Xerophthalmia

    Which one among the following is not correct about Down’s syndrome?

    (a) It is a genetic disorder.

    (b) Affected individual has early aging.

    (c) Effected person has mental retardation.

    (d) The affected person has a furrowed tongue.

    Option b – Affected individual has early aging

    The gene for color blindness is located on

    (a) Y-chromosome

    (b) 13th chromosome

    (c) X-chromosome

    (d) 21st chromosome

    Option c – X-chromosome

    Hemophilia is a genetic disorder that leads to

    (a) a decrease in hemoglobin levels.

    (b) rheumatic heart disease.

    (c) decrease in WBC.

    (d) prevent the clotting of blood.

    Option d – prevent the clotting of blood

    In the context of genetic disorders, consider the following. A woman suffers from color blindness, while her husband does not suffer from it. They have a son and a daughter. In this context, which one of the following statements is most probably correct?

    (a) Both children suffer from color blindness.

    (b) Daughter suffers from color blindness while son does not suffer from it.

    (c) Both children do not suffer from color blindness.

    (d) Son suffers from color blindness, while daughter does not suffer from it.

    Option d – Son suffers from color blindness, while daughter does not suffer from it

    Down’s syndrome is characterized by

    (a) 21st trisomy

    (b) two X and Y-chromosomes

    (c) 19 trisomy

    (d) only one X-chromosome

    Option a – 21st trisomy

    Gaucher’s disease is associated with abnormal metabolism of

    (a) fat

    (b) nucleic acid

    (c) protein

    (d) carbohydrate

    Option a – fat

    The absence of the Y-chromosome in human beings causes

    (a) Turner’s syndrome

    (b) Klinefelter’s syndrome

    (c) Down’s syndrome

    (d) No abnormality

    Option a – Turner’s syndrome

    Who synthesized DNA in vitro?

    (a) Arthur Kornberg

    (b) Robert Hooke

    (c) Edward Jenner

    (d) Joseph Lister

    Option a – Arthur Kornberg

    Who proposed the 3-D helical DNA model?

    (a) Franklin and Wilkins

    (b) Watson and Crick

    (c) Yanofsky

    (d) Meselson and Stani

    Option b – Watson and Crick

    DNA as genetic material was proved by

    (a) Altman

    (b) McLeod

    (c) Fredrick Meischer

    (d) Griffith

    Option d – Griffith

    In the genetic dictionary, there are 64 codons because

    (a) 64 amino acids are to be coded

    (b) 64 types of tRNA are present

    (c) there are 44 non-sense codons and 20 sense codons

    (d) the genetic code is triplet

    Option d – the genetic code is triplet

    The formation of RNA (mRNA) over a DNA template is called

    (a) translation

    (b) transcription

    (c) reverse transcription

    (d) initiation

    Option b – transcription

    Which of the following features of DNA makes it unequally suited to store and transmit genetic information from generation to generation?

    (a) Complementarity of the two strands

    (b) Double helix

    (c) Number of base pairs per turn

    (d) Sugar-phosphate backbone

    Option b – Double helix

    The number of DNA molecules per chromatid is

    (a) one

    (b) two

    (c) three

    (d) four

    Option b – two

    The nucleosome is

    (a) histone proteins

    (b) DNA wrapped around histones

    (c) RNA wrapped around histones

    (d) DNA wrapped around acidic protein

    Option b – DNA wrapped around histones

    In prokaryotes, multiple ribosomes (polysomes) participate in

    (a) translation process

    (b) transcription process

    (c) linkage

    (d) crossing over

    Option a – translation process

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