Molecular cloning and characterization of a novel splice variant of the LIM domain family gene, PINCH 2, in human testis

被引:3
|
作者
Liu, Yun
Liu, Jin
Chen, Jie
Cheng, Libo
Cao, Qinhong
Zhu, Li
Sun, Yan
Liu, Qinghuai
Li, Jianmin
机构
[1] Nanjing Med Univ, Dept Cell Biol & Med Genet, Inst Stomatol, Nanjing 210029, Peoples R China
[2] Nanjing Med Univ, Dept Cell Biol & Med Genet, Lab Reprod Med, Nanjing 210029, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp, Dept Geratol, Nanjing 210008, Peoples R China
[4] Nanjing Med Univ, Affiliated Hosp, Dept Ophthalmol, Nanjing 210008, Peoples R China
关键词
gene; PINCH; 2; LIM domain; testis; spermatogenesis;
D O I
10.1007/BF02686105
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
By hybridizing human adult testis cDNA microarrays with human adult and embryo testis cDNA probes, we identified a novel human testis gene, PINCH 2. PINCH 2 expression was 3.4-fold higher in adult than in fetal testis. The full length of its cDNA was 963 bp, with a 345-bp open reading frame (ORF), encoding a 117-amino acid protein. PINCH 2 was a splicing isoform of PINCH. It shared one exon, which encoded the LIM domain, with PINCH gene in human genome. Multitissue reverse transcriptase-polymerase chain reaction (RTPCR) analysis revealed that this gene was expressed variably in a wide range of tissues, with high expression levels in human adult testis. These results suggest that PINCH 2, a novel LIM domain-containing gene, may play an important role in testicular development/spermatogenesis.
引用
收藏
页码:109 / 118
页数:10
相关论文
共 50 条
  • [31] Molecular Cloning and Characterization of the Human ErbB4 Gene: Identification of Novel Splice Isoforms in the Developing and Adult Brain
    Tan, Wei
    Dean, Michael
    Law, Amanda J.
    PLOS ONE, 2010, 5 (09):
  • [32] Molecular cloning of a novel human acid phosphatase gene (ACPT) that is highly expressed in the testis
    Yousef, GM
    Diamandis, M
    Jung, K
    Diamandis, EP
    GENOMICS, 2001, 74 (03) : 385 - 395
  • [33] Molecular cloning and characterization of a novel human gene containing ankyrin repeat and double BTB/POZ domain
    Dai, KS
    Wei, W
    Liew, CC
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 273 (03) : 991 - 996
  • [34] A SINGLE ANCESTRAL GENE OF THE HUMAN LIM DOMAIN ONCOGENE FAMILY LMO IN DROSOPHILA - CHARACTERIZATION OF THE DROSOPHILA DLMO GENE
    ZHU, TH
    BODEM, J
    KEPPEL, E
    PARO, R
    ROYERPOKORA, B
    ONCOGENE, 1995, 11 (07) : 1283 - 1290
  • [35] Molecular cloning and characterization of a novel human Rab (Rab2B) gene
    Ni, XH
    Ma, YS
    Cheng, HP
    Jiang, M
    Guo, LC
    Ji, CN
    Gu, SH
    Cao, YQ
    Mao, YM
    JOURNAL OF HUMAN GENETICS, 2002, 47 (10) : 548 - 551
  • [36] Molecular cloning and characterization of a novel human Rab (Rab2B) gene
    X. Ni
    Y. Ma
    H. Cheng
    M. Jiang
    L. Guo
    C. Ji
    S. Gu
    Y. Cao
    Y. Xie
    Y. Mao
    Journal of Human Genetics, 2002, 47 : 548 - 551
  • [37] CDNA CLONING OF AN ORPHAN OPIATE RECEPTOR GENE FAMILY MEMBER AND ITS SPLICE VARIANT
    WANG, JB
    JOHNSON, PS
    IMAI, Y
    PERSICO, AM
    OZENBERGER, BA
    EPPLER, CM
    UHL, GR
    FEBS LETTERS, 1994, 348 (01) : 75 - 79
  • [38] Molecular cloning and characterization of SGT1.2, a novel splice variant of Homo sapiens SGT1
    Zou, XQ
    Ji, CN
    Wang, L
    Wu, MQ
    Zheng, HR
    Xu, J
    Jin, F
    Gu, SH
    Ying, K
    Xie, Y
    Mao, YM
    DNA SEQUENCE, 2004, 15 (02): : 140 - 143
  • [39] Identification, characterization and cloning of SLC6A8C, a novel splice variant of the creatine transporter gene
    Martinez-Munoz, Cristina
    Rosenberg, Efraim H.
    Jakobs, Cornelis
    Salomons, Gajja S.
    GENE, 2008, 418 (1-2) : 53 - 59
  • [40] Characterization of a novel five-transmembrane domain cholecystokinin-2 receptor splice variant identified in human tumors
    Sanchez, Claire
    Escrieut, Chantal
    Clerc, Pascal
    Gigoux, Veronique
    Waser, Beatrice
    Reubi, Jean Claude
    Fourmy, Daniel
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2012, 349 (02) : 170 - 179