Botany MCQs for NEET — Practice Questions with Answers

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The mechanism that causes a gene to move from one linkage group to another is called 

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Explanation

Translocation is the process causing a gene to move from one linkage group to another. It is the separation of a chromosome segment and its union to a non-homologous chromosome. It is of two types - Simple and  reciprocal.

In simple translocation one chromosome shows deletion of deficiency while a non-homologous chromosome comes to have an additional segment. In reciprocal translocation two non-homologous chromosomes exchange segments between themselves to create new linkage groups in both the chromosomes. 

Hence, option is correct.

A true breeding plant is

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Explanation

(c) A true breeding plant (pureline) has homozygous genes for a character (e.g., TT for tall or tt for dwarf). It always produces offsprings which are true (pure) for its characters.

The term "linkage" was coined by :-

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Explanation

The term linkage was coined by TH Morgan. He carried out several dihybrid crosses in Drosophila to study genes that were sex-linked. He described the physical association of genes on a chromosome.

The movement of a gene from one linkage group to another is called

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Explanation

(b) The movement of a gene from one linkage group to another is called translocation. It is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes.

Multiple alleles are present 

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Explanation

(c) Mutiple alleles is a condition where a gene exist in more than two allelic forms that are present on the same locus of the chromosome. For eg : ABO system in humans.

Which one of the following cannot be explained on the basis of Mendel's Law of Dominance?

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Explanation

The law of dominance does not occur universally. After Mendel several cases were recorded by scientists, where a clear deviation from law of dominance was seen in the form of incomplete dominance or Blending inheritance and Co-dominance. 

Where F1 generation hybrids exhibited a mixture or blending of character of two parents, the case is considered as that of incomplete dominance blending inheritance. It is simply means that two genes of allelomorphic pair are not related as dominant or recessive, but each of them expresses itself partially. In the case of 4 o'clock plant, when plants with red flowers are crossed with plants having white flower, the F1 hybrids bear pink flowe. When these pink flowers are self pollinated, they develop red, pink and white flowers in the ratio of 1 : 2 : 1 respectively. 

The genotype of a plant showing the dominant phenotype can be determined by

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Explanation

In genetics, a test cross, first introduced by Gregor Mendel, is used to determine if an individual exhibiting a dominant trait is homozygous or heterozygous for that trait. More simply, test cross determines the genotype of an individual with a dominant phenotype. In some sources, the test cross is defined as being a type of back cross between the recessive homozygote and F1 generation.

ABO blood groups in humans are controlled by the gene I. It has three alleles — IA, IB and i. Since there are three different alleles, six different genotypes are possible. How many phenotypes can occur?

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Explanation

In ABO blood groups system, inheritance of grouping is controlled by a single autosomal gene on chromosome 9 with three major alleles A, B and O ( IA, IB and iO). The ABO blood group system has at least 6 genotypes. on the basis of presence or absence of antigens and antibodies, four blood groups (phenotypes) have been differentiated — A, B, AB and O blood groups. 

Select the correct statement from the ones given below with respect to dihybrid cross.

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Explanation

Recombination is a rearrangement of genes during meiosis so that a gamete contains a haploid genotype with a new gene combination. Morgan and his group found that when genes were grouped on the same chromosome, some genes were very tightly linked (showed very low recombination), while others were loosely linked (showed higher recombination).

Inheritance of skin colour in humans is an example of :

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Explanation

Inheritance of skin colour in humans is the result of polygenic inheritance or multiple factor inheritance. The inheritance of human skin colour was studied by C.B. Davenport in 1913.

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