Evidence map›Paper›PMID 19203997›Full record

ArticleThe Journal of biological chemistry2009

The death domain of FADD is essential for embryogenesis, lymphocyte development, and proliferation.

Hongxia Z Imtiyaz, Xiaohui Zhou, Haibing Zhang, Dehua Chen, Taishan Hu, Jianke Zhang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. FADD as a key molecular player in cancer progression.Molecular medicine (Cambridge, Mass.) · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Developmental checkpoints guarded by regulated necrosis.Cellular and molecular life sciences : CMLS · 2016
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Hongxia Z ImtiyazDepartment of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107 and Wenzhou Medical College, Zhejiang, China 325035.
Xiaohui Zhou
Haibing Zhang
Dehua Chen
Taishan Hu
Jianke Zhang
Thomas Jefferson University · USWenzhou Medical University · CN

Funding

Apoptosis and Proliferation Signaling Mediated by FADDR01CA095454 · NCI · THOMAS JEFFERSON UNIVERSITY · PI ZHANG, JIANKE · 2002 to 2006
$1.4M
NCI NIH HHS R01 CA95454
6 · The paper itself

Abstract

The Fas-associated death domain-containing protein (FADD) is an adaptor for relaying apoptotic signals initiated by death receptors such as Fas. Whereas a lack of death receptors has no effect on mouse development, FADD deficiency results in early embryonic lethality, indicating that FADD has additional functions independent of death receptors. We have previously shown that conditional deletion of FADD not only impairs apoptosis but also leads to defective lymphocyte proliferation. The non-apoptotic signaling mediated by FADD remains poorly understood. Earlier studies have suggested that FADD carboxyl terminal serine phosphorylation likely plays a role in FADD-mediated proliferation signaling in T cells. The FADD death domain is presumably only required for apoptotic signaling, as it interacts with death receptors which are dispensable during embryonic development and lymphocyte proliferation. To test this hypothesis, we have performed mutational analyses of the FADD death domain and identified a mutant, R117Q, which lacks binding to Fas and, thus, is incapable of apoptotic signaling in cell lines. Unexpectedly, this death domain point mutation disrupted mouse embryonic development as shown by in vivo functional reconstitution analyses. Interestingly, a second FADD death domain mutant, V121N, retained normal Fas binding and apoptotic signaling ability but also failed to support mouse development. Furthermore, lymphocyte proliferation responses were impaired by V121N. This reverse genetic study has revealed a previously unappreciated role of the FADD death domain, which likely functions as a molecular switch regulating two distinct signals leading to apoptosis and cell proliferation and is critical for embryogenesis, lymphocyte development, and proliferation.

Indexed as

Gene Expression Regulation, DevelopmentalAmino Acid SequenceAnimalsApoptosisCell ProliferationFas-Associated Death Domain ProteinLymphocytesMiceMolecular Sequence DataPhosphorylationPoint MutationProtein BindingProtein Structure, TertiarySequence Homology, Amino AcidT-LymphocytesFas-Associated Death Domain Protein

Identifiers

PMID19203997
PMCPMC2665115
OpenAlexW2051717975

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.