TLS Online TPP Program

#Question id: 10378


Nod factor as signaling agents binds with the nod factor receptor NFR on the basis for host–symbiont specificity, which of the following is incorrect?

#Unit 6. System Physiology – Plant
  1. NFR is an heterodimer in the cytosolic side that is NFR1 and NFR5
  2. The receptor contains two domain lysin motifs (LysM) in the extracellular domain and kinase domain in the cytosolic side
  3. Receptor contain intracellular domains with similarity to plant serine/threonine protein kinases, but only NFR2 has kinase activity
  4. Lysine of LysM is not consider as amino acid it refer to an enzyme that hydrolyzes bacterial peptidoglycan walls
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TLS Online TPP Program

#Question id: 5370

#Unit 8. Inheritance Biology

The pedigree below represents the inheritance of an X link recessive trait. The probability of effected child in fourth generation of family?

TLS Online TPP Program

#Question id: 5369

#Unit 8. Inheritance Biology

Above family shows inheritance of colour-blindness is recessive genetic disorder. Which of the following is correct statement? (All persons are outside of family either homozygous (female) or hemizygous (Male) are consider)

TLS Online TPP Program

#Question id: 5368

#Unit 8. Inheritance Biology

Which of the following is correct about genetic disorder in family?

A) Gene for this trait present in both sex

B) Trait is governed by mitochondrial gene

C) Sex limited trait acts like a recessive trait on an autosome

D) Sex influenced trait acts like a dominant trait on an autosome

TLS Online TPP Program

#Question id: 5367

#Unit 8. Inheritance Biology

Following pedigree showing X link recessive disorder. Which of the following confirm a carrier female in a family?

TLS Online TPP Program

#Question id: 5366

#Unit 8. Inheritance Biology

From the following select the possible mode of inheritance and the probability that the child in generation III will show the trait.

TLS Online TPP Program

#Question id: 5365

#Unit 8. Inheritance Biology

The following pedigree shows the inheritance of a common phenotype controlled by an autosomal recessive allele. The probability of carriers in the population is 1/3. What is the probability that a child from parents III-3 and III-4 will show the phenotype?