Pregled bibliografske jedinice broj: 37292
Transcription factors of the zinc finger family in human disorders
Transcription factors of the zinc finger family in human disorders // Annual meeting of the Croatian immunological society
Zagreb, 1999. (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 37292 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Transcription factors of the zinc finger family in human disorders
Autori
Kušić, Borka ; Gršković, Marica ; Herak Bosnar, Maja ; Bačić, Sanja ; Dominis, Marija ; Antica, Mariastefania
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Annual meeting of the Croatian immunological society
/ - Zagreb, 1999
Skup
Annual meeting of the Croatian immunological society
Mjesto i datum
Zagreb, Hrvatska, 25.11.1999
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
transcription factors; human malignancies; lymphocytes
Sažetak
Development of the lymphoid system is dependent on the activity of a transcription factor family encoded by Ikaros, Aiolos and Helios genes. These transcription factors are alternative splicing variants of primary RNA transcripts and they belong to the family of zinc finger proteins that specifically bind to DNA. It has been shown in mice that dimerization deficient isoforms of at least one of these transcription factors, the Ikaros gene, fail to transactivate target genes, and lead to lymphoproliferation and lymphoma development. On the other hand some authors found that Ikaros and related proteins can repress transcription from specific promotors in a cell type dependent manner. The aim of the present study is to analyse human lymphoid malignancies in order to check weather Ikaros, Aiolos or Helios expression in these disorders is impaired. By means of RT-nested-PCR method and specific primers for these genes we analysed their expression in human lymphoid cell lines (Jurkat, MOLT, NALM) and in lymph nodes from Hodgkins and Non-Hodgkins lymphoma patients. Our results show Ikaros expression in all tested samples. We found Aiolos being differentially expressed in adult human lymphoma. In 10 out of 18 lymphoma, Aiolos transcripts were detected. An additional smaller transcript was apparent in one of these lymphoma specimens. However even in the cases, where transcripts were detected, it is possible they are unfunctional splicing variants resulting from point mutations. Sequencing of the transcripts will give us more insight in the nature of transcripts and their relevance in lymphoproliferative disease development.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
00981101
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Marija Dominis
(autor)
Maja Herak Bosnar
(autor)
Mariastefania Antica
(autor)
Borka Kušić
(autor)