Literature DB >> 8378095

C-ski transcripts with and without exon 2 are expressed in skeletal muscle and throughout chick embryogenesis.

H L Grimes1, M R Ambrose, M M Goodenow.   

Abstract

Overexpression of v-ski or c-ski cDNAs has a pronounced effect on proliferation, morphological transformation and myogenic differentiation in cells in culture and in transgenic animals. Yet, little is known about expression of the c-ski locus or the relationship between c-ski cDNAs and alternatively spliced c-ski transcripts in chicken tissues, particularly in skeletal muscle or during embryogenesis. We developed a series of probes and oligonucleotide primers specific for the eight coding exons and the long 3' noncoding region found in chicken c-ski mRNAs. The most abundant chicken c-ski mRNAs in a vast array of tissues are 8.5 kb, with additional, but less abundant, mRNAs of 7.5, 6.5 and 4.4 kb. Steady-state levels of c-ski mRNAs, indistinguishable from transcripts in other tissues, accumulate in skeletal muscle from embryonic, newly hatched, and adult chicks. Only exon 2, a small exon of 111 bp, was found to be alternatively spliced in c-ski mRNAs. Transcripts with and without exon 2 appear in all tissues, in somites, and from the earliest stages of chick embryogenesis. Thus, c-ski cDNA sequences, which extend about 4.3 kb, represent either the least abundant form of c-ski mRNAs in tissues or a severely truncated form of the major 8.5 kb transcripts.

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Year:  1993        PMID: 8378095

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  6 in total

1.  Proto-oncogene Sno expression, alternative isoforms and immediate early serum response.

Authors:  S Pearson-White; R Crittenden
Journal:  Nucleic Acids Res       Date:  1997-07-15       Impact factor: 16.971

2.  Somatic cell mapping of the SKI proto-oncogene to bovine syntenic group U25 (BTA 27)

Authors:  A M Ryan; J E Womack
Journal:  Mamm Genome       Date:  1995-08       Impact factor: 2.957

3.  Mice lacking the ski proto-oncogene have defects in neurulation, craniofacial, patterning, and skeletal muscle development.

Authors:  M Berk; S Y Desai; H C Heyman; C Colmenares
Journal:  Genes Dev       Date:  1997-08-15       Impact factor: 11.361

4.  SKI controls MDS-associated chronic TGF-β signaling, aberrant splicing, and stem cell fitness.

Authors:  David E Muench; Kyle Ferchen; Chinavenmeni S Velu; Kith Pradhan; Kashish Chetal; Xiaoting Chen; Matthew T Weirauch; Clemencia Colmenares; Amit Verma; Nathan Salomonis; H Leighton Grimes
Journal:  Blood       Date:  2018-09-24       Impact factor: 22.113

5.  Induction of Ski Protein Expression upon Luteinization in Rat Granulosa Cells.

Authors:  Hyun Kim; Dong Hun Kim; Soo Bong Park; Yeoung-Gyu Ko; Sung-Woo Kim; Yoon Jun Do; Jae-Hong Park; Boh-Suk Yang
Journal:  Asian-Australas J Anim Sci       Date:  2012-05-01       Impact factor: 2.509

6.  Transcriptional cofactors Ski and SnoN are major regulators of the TGF-β/Smad signaling pathway in health and disease.

Authors:  Angeles C Tecalco-Cruz; Diana G Ríos-López; Genaro Vázquez-Victorio; Reyna E Rosales-Alvarez; Marina Macías-Silva
Journal:  Signal Transduct Target Ther       Date:  2018-06-08
  6 in total

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