Evidence map›Paper›PMID 24981926›Full record

ArticleMolecular biology reports2014

Characterization of human gene locus CYYR1: a complex multi-transcript system.

Raffaella Casadei, Maria Chiara Pelleri, Lorenza Vitale, Federica Facchin, Silvia Canaider, Pierluigi Strippoli, Matteo Vian, Allison Piovesan, Eva Bianconi, Elisa Mariani and 2 more

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Article in Molecular biology reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Raffaella CasadeiDepartment for Life Quality Studies, University of Bologna, C.so d'Augusto 237, 47921, Rimini, RN, Italy.
Maria Chiara Pelleri
Lorenza Vitale
Federica Facchin
Silvia Canaider
Pierluigi Strippoli
Matteo Vian
Allison Piovesan
Eva Bianconi
Elisa Mariani
Francesco Piva
Flavia Frabetti
University of Bologna · ITMarche Polytechnic University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cysteine/tyrosine-rich 1 (CYYR1) is a gene we previously identified on human chromosome 21 starting from an in-depth bioinformatics analysis of chromosome 21 segment 40/105 (21q21.3), where no coding region had previously been predicted. CYYR1 was initially characterized as a four-exon gene, whose brain-derived cDNA sequencing predicts a 154-amino acid product. In this study we provide, with in silico and in vitro analyses, the first detailed description of the human CYYR1 locus. The analysis of this locus revealed that it is composed of a multi-transcript system, which includes at least seven CYYR1 alternative spliced isoforms and a new CYYR1 antisense gene (named CYYR1-AS1). In particular, we cloned, for the first time, the following isoforms: CYYR1-1,2,3,4b and CYYR1-1,2,3b, which present a different 3' transcribed region, with a consequent different carboxy-terminus of the predicted proteins; CYYR1-1,2,4 lacks exon 3; CYYR1-1,2,2bis,3,4 presents an additional exon between exon 2 and exon 3; CYYR1-1b,2,3,4 presents a different 5' untranslated region when compared to CYYR1. The complexity of the locus is enriched by the presence of an antisense transcript. We have cloned a long transcript overlapping with CYYR1 as an antisense RNA, probably a non-coding RNA. Expression analysis performed in different normal tissues, tumour cell lines as well as in trisomy 21 and euploid fibroblasts has confirmed a quantitative and qualitative variability in the expression pattern of the multi-transcript locus, suggesting a possible role in complex diseases that should be further investigated.

Indexed as

Alternative SplicingAmino Acid SequenceComputer SimulationExonsGene ExpressionGenesGenetic LociHumansMembrane ProteinsMolecular Sequence DataOrgan SpecificityProtein IsoformsCYYR1 protein, humanMembrane ProteinsProtein Isoforms

Identifiers

PMID24981926
OpenAlexW2326265172

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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.