Related Experiment Video
Updated: Jun 24, 2026

08:43
Loss- and Gain-of-function Approach to Investigate Early Cell Fate Determinants in Preimplantation Mouse Embryos
Published on: June 6, 2016
Cyclin T2 is essential for mouse embryogenesis.
Jiri Kohoutek1, Qintong Li, Dalibor Blazek
1Veterinary Research Institute, Hudcova 70, 621 00, Brno, Czech Republic. kohoutek@vri.cz
Molecular and Cellular Biology
|April 15, 2009
Summary
Cyclin T2 (CycT2) is crucial for embryonic development, not redundant with Cyclin T1 (CycT1). Inactivating the CycT2 gene leads to early embryonic lethality, highlighting distinct gene regulation by P-TEFb complexes.
Area of Science:
- Molecular Biology
- Developmental Biology
- Genetics
Background:
- The positive transcription elongation factor b (P-TEFb) complex, comprising cyclin T (CycT) and cyclin-dependent kinase 9 (Cdk9), is vital for RNA polymerase II transcription elongation.
- Mammalian P-TEFb exists with either Cyclin T1 (CycT1) or Cyclin T2 (CycT2), raising questions about their functional redundancy.
Purpose of the Study:
- To investigate whether CycT1 and CycT2 have redundant functions or regulate distinct gene sets.
- To determine the role of CycT2 in embryonic development through genetic inactivation.
Main Methods:
- Genetic inactivation of the CycT2 gene (Ccnt2) in mice using beta-galactosidase-neomycin (beta-geo) gene trap technology.
- Visualization of beta-galactosidase expression during mouse embryogenesis and in adult tissues.
- Assessment of CycT2 function in embryonic stem cells using short interfering RNAs (siRNAs).
Main Results:
- CycT2 exhibits widespread expression during embryogenesis and in all adult tissues and organs.
- Homozygous inactivation of CycT2 (CycT2-/-) resulted in early embryonic lethality, with no viable offspring.
- siRNA-mediated knockdown of CycT2 in embryonic stem cells indicated downregulation of critical genes.
Conclusions:
- CycT1 and CycT2 are not functionally redundant.
- Distinct P-TEFb complexes formed by CycT1 and CycT2 regulate separate subsets of genes essential for embryonic development.
Related Concept Videos
Meiosis II
Meiosis II entails cell division and segregation of the sister chromatids, resulting in the production of four unique haploid gametes. The steps for meiosis II are similar to mitosis, except that meiosis II occurs in haploid cells, whereas mitosis occurs in diploid cells.
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
Meiosis II
Meiosis II is the second and final stage of meiosis. It relies on the haploid cells produced during meiosis I, each of which contain only 23 chromosomes—one from each homologous initial pair. Importantly, each chromosome in these cells is composed of two joined copies, and when these cells enter meiosis II, the goal is to separate such sister chromatids using the same microtubule-based network employed in other division processes. The result of meiosis II is two haploid cells, each containing...
M-Cdk Drives Transition Into Mitosis
Checkpoints throughout the cell cycle serve as safeguards and gatekeepers, allowing the cell cycle to progress in favorable conditions and slow or halt it in problematic ones. This regulation is known as the cell cycle control system.
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
Positive Regulator Molecules
Mitotic cell division results in daughter cells that exactly resemble the parent cell. However, errors in the DNA replication or distribution of genetic material may lead to genetic mutations that may be passed down to every new cell formed from the resulting abnormal cell. Propagation of such mutant cells is restricted through checkpoint mechanisms present at different stages of the cell cycle. These checkpoints involve regulator molecules that either promote or demote cell cycle events.
Positive Regulator Molecules
To consistently produce healthy cells, the cell cycle—the process that generates daughter cells—must be precisely regulated.
Mitogens and the Cell Cycle
Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...

