Reference SummaryAllen CE, Genes Chromosomes Cancer 2002 Dec;35(4):287-98

Title

Developmental anomalies and neoplasia in animals and cells deficient in the large zinc finger protein KRC.

Authors

Allen CE; Muthusamy N; Weisbrode SE; Hong JW; Wu LC

Journal

Genes Chromosomes Cancer

Volume

35

Issue

4

Year

2002

Pages

287-98

Abstract

The large zinc finger protein KRC binds to the signal sequences of V(D)J recombination and the kappaB motif. Disruption of KRC expression in cell lines resulted in increased cell proliferation, anchorage independence of growth, and uncoupling of nuclear division and cell division. In this report, the function of KRC was studied in a RAG2-deficient blastocyst complementation animal model. KRC-deficient embryonic stem cells were generated by homologous recombination and were introduced into RAG2(-/-) blastocysts to generate KRC(-/-);RAG2(-/-) chimeric mice. The lymphoid compartments of chimeras examined at 5 weeks of age were developed, suggesting that KRC is not essential for V(D)J recombination development. However, by 6 months of age, there was a marked deficit in CD4(+)CD8(+) thymocytes in the chimeras, suggesting that KRC may be involved in T-lymphocyte survival. Additionally, one chimera developed anomalies, including postaxial polydactyly, hydronephrosis, and an extragonadal malignant teratoma. DNA analysis showed that the teratoma was derived from KRC(-/-) embryonic stem cells. The teratoma had compound tissue organization and was infiltrated with B lymphocytes. Subsequently, several immortalized KRC-deficient cell lines were established from the teratoma. In this study, growth anomalies and neoplasia were observed in animals and cells deficient in KRC, and other studies have shown allelic loss occurring at the chromosomal region of the human KRC counterpart in various tumors. We propose that KRC may be a previously unidentified tumor-suppresser gene. Copyright 2002 Wiley-Liss, Inc.

Links

J:79652 – MGI References
12378523 – National Library of Medicine/PubMed

Models

Strain Model Name Treatment Agent(s) Organ Affected Frequency Model Details
B6.129S6-Rag2tm1Fwa : 129X1/SvJ-Hivep3tm1Lcw Germ cell (sex not specified) teratocarcinoma Germ cell (sex not specified)

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