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The Pristionchus HOX gene Ppa-lin-39 inhibits programmed cell death to specify the vulva equivalence group and is not required during vulval induction

MPG-Autoren
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Sommer,  RJ       
Department Cell Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Eizinger,  A
Department Cell Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Lee,  K-Z
Department Cell Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Jungblut,  B       
Department Cell Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Bubeck,  A
Department Cell Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Schlak,  I
Department Cell Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Zitation

Sommer, R., Eizinger, A., Lee, K.-Z., Jungblut, B., Bubeck, A., & Schlak, I. (1998). The Pristionchus HOX gene Ppa-lin-39 inhibits programmed cell death to specify the vulva equivalence group and is not required during vulval induction. Development, 125(19), 3865-3873. doi:10.1242/dev.125.19.3865.


Zitierlink: https://hdl.handle.net/21.11116/0000-000D-C14A-6
Zusammenfassung
In the two nematode species Caenorhabditis elegans and Pristionchus pacificus the vulva equivalence group in the central body region is specified by the Hox gene lin-39. C. elegans lin-39 mutants are vulvaless and the vulval precursor cells fuse with the surrounding hypodermis, whereas in P. pacificus lin-39 mutants the vulval precursor cells die by apoptosis. Mechanistically, LIN-39 might inhibit non-vulval fate (cell fusion in C. elegans, apoptosis in P. pacificus), promote vulval fate or do both. To study the mechanism of lin-39 function, we isolated P. pacificus cell death mutants and identified mutations in ced-3. Surprisingly, P. pacificus ced-3; lin-39 double mutants form a functional vulva in the absence of LIN-39 activity. Thus, in P. pacificus lin-39 specifies the vulva equivalence group by inhibiting programmed cell death. Furthermore, these data reveal an important difference in a later function of lin-39 between the two species. In C. elegans, LIN-39 specifies vulval cell fates in response to inductive RAS signaling, and in P. pacificus LIN-39 is not required for vulval induction. Thus, the comparative analysis indicates that lin-39 has distinct functions in both species although the gene is acting in a homologous developmental system.