Crown gall properties — Once induced by Agrobacterium, what are the in vitro characteristics of crown gall tissue?

Biotechnology Gene Transfer in Plants Difficulty: Easy
Choose an option
  • A
    It can be cultivated in vitro in the absence of bacteria
  • B
    It retains tumorous properties when cultivated (hormone-autotrophic growth and opine production)
  • C
    Both (a) and (b)
  • D
    It shows tumorous properties only in the presence of the bacteria
  • E
    It rapidly reverts to normal without T-DNA

Answer

Correct Answer: Both (a) and (b)

Explanation

Introduction / Context:Crown gall results from stable integration of T-DNA into the plant genome. After transformation, the tissue becomes autonomous: it can grow without Agrobacterium and often without exogenous hormones, reflecting the expression of T-DNA oncogenes and opine synthesis genes.

Given Data / Assumptions:

  • T-DNA integration is stable and heritable in cultured cells.
  • Opine synthesis and auxin/cytokinin biosynthesis genes alter metabolism and growth control.
  • Eliminating the bacteria does not remove the integrated T-DNA.

Concept / Approach:Because the tumor phenotype is encoded by plant-integrated T-DNA, crown gall tissue remains tumorous in culture without the bacterium. This autonomy is a cornerstone of Agrobacterium-mediated transformation evidence.

Step-by-Step Solution:

Induction: Agrobacterium transfers T-DNA → integration.Post-induction culture: remove bacteria; tissue still grows aberrantly.Conclusion: both independence from bacteria and retention of tumor traits occur.

Verification / Alternative check:Opine assays and hormone-free growth of tumor lines confirm persistent T-DNA function.

Why Other Options Are Wrong:

d) Incorrect; tumor properties do not require persistent bacteria.e) Reversion requires loss/silencing of T-DNA, which is not the default.

Common Pitfalls:Assuming antibiotic curing of bacteria will cure the tumor; integrated T-DNA remains.

Final Answer:Both (a) and (b).

Discussion & Comments
No comments yet. Be the first to comment!
Join Discussion