P 369 Phospholipase C: A candidate for human retinal degeneration

نویسندگان

  • Robert E. Anderson
  • Abboud J. Ghalayini
  • Richard A. Alvarez
  • Robert Nordquist
  • Wolfgang Baehr
چکیده

The retina contains due families of phspbolipnsc C (P, 6. and u). a reccctor-activated ewYmC that PFeratcs two iolraceUuhv s%xmd n&cngcrs, diacylgly&ol md I ,$5-inositol rrispbospbale. We hnvc charactaizcd the cDNA and par&d gene sh-ucnue for human PLCB4, a p isofurm which shares uighcsr sequence homology with dx norpA PLC from Drosophila. A muwion in tie nor@ PU: leads m I retinal demmtioo m dte flv. Immunobtot and immunowtocbem~cal analyses w&c carried au, onbovioc, monkey, “d huti mhlv and reti& membranes with a pcptidc-specific antitidies (Ab) 0 d~c C-tznniou~ of bovioe PLCp4. hnmuwbtot analysi of whole human rctioa membranes shvcd, 130 kDa immonorcactivc protein and a less abundmt 150-160 kDa pmtcin hnmwhesninl &ia showed immunoreacdon in tic photmxquor cell bya md the outa plcxifoml mu layer of bovine rctbu The compositccDNA xquenec derived from several overtapping cDNA &,,us &,,rh,,w,,, dnd Library predicis a hunus PLCp4 polypeplidc of ,022 amino acid residues (mw. I17.000). Illis PLQ34 variant tacks P 165 mdno ,&I N-tcrminnl domiC chvactaistic for the mt bhin imro,m, but bz,s , disdnc, putivc cxon I “niqw for bun= and bovine mdm iwfomu. Humps gcnomic DNA ws mqdifed witi cxoo specific primers to map intxonlcxon juncdon8. The I34 gme conti yl ioUOOLess purativc cxon t hagmcnt mntihg PI and the lranstatioo EM codon. I,, addition exon 2 (95 bp) and cxoo 3 (58 bp), IS well IS invon 1 (I kb) u,d iomn h (0.6 kb) bwe hem wped. Exon 3 ~rrcyponds to Ox P3 slice varianr. Somatic cell hybrids. and d&lion panels were used u, bmlizc Ihe m34 gco~ IO die &orI arm of chromosome 20. ‘The gcnc was 6mbcr sublocalized (0 20~12 by fluOrc~cco~e in situ hybridndon.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Identification of candidate genes for human retinal degeneration loci using differentially expressed genes from mouse photoreceptor dystrophy models

PURPOSE Retinal degeneration (RD) is a complex mechanism that appears to involve many biologic processes including oxidative stress, apoptosis, and cellular remodeling. Currently there are 51 mapped, but not identified, RD human disease loci. METHODS To assign possible disease genes to RD loci, we have used a comparative genomics procedure that incorporates microarray gene expression data of ...

متن کامل

Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Cumbs homologue 1) Mutations in Iranian Retinal Degeneration Families

Background: Inherited retinal diseases (IRDs) are a group of genetic disorders with high degrees of clinical, genetic and allelic heterogeneity. IRDs generally show progressive retinal cell death resulting in gradual vision loss. IRDs constitute a broad spectrum of disorders including retinitis pigmentosa and Leber congenital amaurosis. In this study, we performed genotyping studies to identify...

متن کامل

Depletion of PtdIns(4,5)P₂ underlies retinal degeneration in Drosophila trp mutants.

The prototypical transient receptor potential (TRP) channel is the major light-sensitive, and Ca(2+)-permeable channel in the microvillar photoreceptors of Drosophila. TRP channels are activated following hydrolysis of phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P₂] by the key effector enzyme phospholipase C (PLC). Mutants lacking TRP channels undergo light-dependent retinal degeneration,...

متن کامل

Loss of the phospholipase C gene product induces massive endocytosis of rhodopsin and arrestin in Drosophila photoreceptors

Previously we have shown that a subset of visual transduction mutants in Drosophila melanogaster induce the formation of stable complexes between rhodopsin and arrestin. One such mutant is in a visual system-specific phospholipase C (PLC). The rhodopsin/arrestin complexes generated in PLC mutants induce massive retinal degeneration. Here we demonstrate that both arrestin and rhodopsin undergo l...

متن کامل

Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness.

Blindness due to retinal degeneration affects millions of people worldwide, but many disease-causing mutations remain unknown. PNPLA6 encodes the patatin-like phospholipase domain containing protein 6, also known as neuropathy target esterase (NTE), which is the target of toxic organophosphates that induce human paralysis due to severe axonopathy of large neurons. Mutations in PNPLA6 also cause...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Vision Research

دوره 35  شماره 

صفحات  -

تاریخ انتشار 1995