STRUCTURE AND EXPRESSION OF CHICKEN PROTEIN-KINASE PITSLRE-ENCODING GENES

被引:17
作者
LI, HM
GRENET, J
VALENTINE, M
LAHTI, JM
KIDD, VJ
机构
[1] ST JUDE CHILDRENS RES HOSP, DEPT TUMOR CELL BIOL, MEMPHIS, TN 38105 USA
[2] ST JUDE CHILDRENS RES HOSP, DEPT EXPTL ONCOL, MEMPHIS, TN 38105 USA
关键词
CELL CYCLE; TUMOR SUPPRESSOR; PROTEIN KINASE; APOPTOSIS;
D O I
10.1016/0378-1119(94)00801-X
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The human PITSLRE protein kinases (PK), members of the p34(cdc2) kinase family named according to the single amino acid (aa) code of an important (PSTAIRE) regulatory region [Meyerson et al., EMBO J. 11 (1992) 2909-2917], are candidate tumor suppressor gene(s) localized to human chromosome 1p36.2 and a syntenic region of mouse chromosome 4 [Lahti et al., Nature Genet. 7 (1994) 370-375; Mock et al., Mammal. Genome 5 (1994) 191-192]. At least ten isoforms of this PK family are expressed from three duplicated and tandemly linked genes in humans [Xiang et al., J. Biol. Chem. 269 (1994) 15786-15794]. We have now isolated two different species of PITSLRE PK cDNAs from chicken that encode identical polypeptides, but are clearly expressed from different genes, based on nucleotide (nt) differences. Isolation of one of the corresponding chicken PITSLRE PK genes confirms that only one of the two species of PITSLRE mRNA is expressed from this gene. Comparison of the predicted avian PITSLRE PK aa sequence to human and mouse sequences shows a high degree of sequence identity (>91%). Like humans, the PITSLRE PK genes in chickens must be closely linked, based on fluorescent in situ hybridization (FISH) localization of these genes to a single chicken microchromosome. PITSLRE PK mRNAs are expressed in two avian B- and T-cel lines. These results suggest that the PITSLRE PK gene family has been well conserved evolutionarily, that the gene duplication observed in humans is not a recent event, and that expression of redundant PITSLRE mRNAs is observed in different vertebrate species.
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收藏
页码:237 / 242
页数:6
相关论文
共 26 条
[1]   INCREASED RATIO OF TARGETED TO RANDOM INTEGRATION AFTER TRANSFECTION OF CHICKEN B-CELL LINES [J].
BUERSTEDDE, JM ;
TAKEDA, S .
CELL, 1991, 67 (01) :179-188
[2]   INCREASED EXPRESSION OF A 58-KDA PROTEIN-KINASE LEADS TO CHANGES IN THE CHO CELL-CYCLE [J].
BUNNELL, BA ;
HEATH, LS ;
ADAMS, DE ;
LAHTI, JM ;
KIDD, VJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (19) :7467-7471
[3]   ACTIVATION OF HUMAN CYCLIN-DEPENDENT KINASES INVITRO [J].
DESAI, D ;
GU, Y ;
MORGAN, DO .
MOLECULAR BIOLOGY OF THE CELL, 1992, 3 (05) :571-582
[4]   CDC2 FAMILY KINASES PHOSPHORYLATE A HUMAN CELL-DNA REPLICATION FACTOR, RPA, AND ACTIVATE DNA-REPLICATION [J].
DUTTA, A ;
STILLMAN, B .
EMBO JOURNAL, 1992, 11 (06) :2189-2199
[5]   STRUCTURE AND EXPRESSION OF THE HUMAN P58(CLK-1) PROTEIN-KINASE CHROMOSOMAL GENE [J].
EIPERS, PG ;
LAHTI, JM ;
KIDD, VJ .
GENOMICS, 1992, 13 (03) :613-621
[6]   A NEW HUMAN P34 PROTEIN-KINASE, CDK2, IDENTIFIED BY COMPLEMENTATION OF A CDC28 MUTATION IN SACCHAROMYCES-CEREVISIAE, IS A HOMOLOG OF XENOPUS-EG1 [J].
ELLEDGE, SJ ;
SPOTTSWOOD, MR .
EMBO JOURNAL, 1991, 10 (09) :2653-2659
[7]   CDK2 ENCODES A 33-KDA CYCLIN-A-ASSOCIATED PROTEIN-KINASE AND IS EXPRESSED BEFORE CDC2 IN THE CELL-CYCLE [J].
ELLEDGE, SJ ;
RICHMAN, R ;
HALL, FL ;
WILLIAMS, RT ;
LODGSON, N ;
HARPER, JW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :2907-2911
[8]  
FACCHINI LM, 1994, CELL GROWTH DIFFER, V5, P637
[9]   EVIDENCE THAT THE G1-S AND G2-M TRANSITIONS ARE CONTROLLED BY DIFFERENT CDC2 PROTEINS IN HIGHER EUKARYOTES [J].
FANG, F ;
NEWPORT, JW .
CELL, 1991, 66 (04) :731-742
[10]   THE MO15 GENE ENCODES THE CATALYTIC SUBUNIT OF A PROTEIN-KINASE THAT ACTIVATES CDC2 AND OTHER CYCLIN-DEPENDENT KINASES (CDKS) THROUGH PHOSPHORYLATION OF THR161 AND ITS HOMOLOGS [J].
FESQUET, D ;
LABBE, JC ;
DERANCOURT, J ;
CAPONY, JP ;
GALAS, S ;
GIRARD, F ;
LORCA, T ;
SHUTTLEWORTH, J ;
DOREE, M ;
CAVADORE, JC .
EMBO JOURNAL, 1993, 12 (08) :3111-3121