Some given statements about Auxin signalling pathways are listed;

a) The auxin receptor is composed of two proteins: the SCF complex component TIR1 and the repressor protein AUX/IAA

b) The binding of auxin to its receptor complex initiates ubiquitin-dependent degradation of the AUX/ IAA repressor protein by the 26S proteasome 

c) TIR1 recruits AUX/ IAA proteins to the SCFTIR1  complex in an auxin-independent manner

d) AUX/IAA proteins are ubiquitinated by the E3 ligase activity of the SCFTIR1 complex, which marks the protein for destruction by the 26S proteasome

Which of the following is correct explanation of Auxin signalling pathways?

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#Question id: 3537

#Unit 8. Inheritance Biology

What is the probability of two offspring in which one dominant phenotype and one recessive phenotype from the mating Aa × Aa?

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#Question id: 3538

#Unit 8. Inheritance Biology

Monohybrid cross allowed between heterozygous Rr (Round) and RR (Round), all progeny having Round seeded plant were allowed to self-fertilize to produce numerous progeny that are 

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#Question id: 3542

#Unit 8. Inheritance Biology

All genes are not linked. The probability of a progeny being AaBBccDd from a corss between AABbccDd and aaBBccDD parents will be

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#Question id: 3545

#Unit 8. Inheritance Biology

Consider the accompanying pedigree of a rare autosomal recessive disease, PKU. Male with PKU marry with normal female whose father is PKU. What is probability of child affected with PKU?

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#Question id: 4900

#Unit 8. Inheritance Biology

The chlorophyll-deficient types occur in a particular plant species due to a mutation in the DNA of the chloroplast itself, Female cytoplasm chlorophyll-deficient organisms crossed with male normal chlorophyll will produce progeny

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#Question id: 17809

#Unit 8. Inheritance Biology

In humans, albinism (unpigmented skin, hair, and eyes) is due to an enzymatic deficiency, and it is an autosomal recessive trait. Suppose that in a small country of one million people (“Generation 1”), there are 500 aa albinos and 9000 Aa heterozygous carriers. What is the probability that a child will be albino if: Both parents are members of Generation 2, and one parent is albino and the other is non-albino.