Expression and alternative splicing of the deleted in colorectal cancer (DCC) gene in normal and malignant tissues

M A Reale1, G Hu, A I Zafar

  • 1Department of Medicine, Yale University School of Medicine, New Haven, Connecticut 06536-0812.

Cancer Research
|August 15, 1994
PubMed

Insights

The deleted in colorectal cancer (DCC) gene encodes glycoproteins. DCC expression is highest in brain tissues but reduced in most cancer cell lines, suggesting potential genetic inactivation in tumors.

Area of Science:

  • Molecular Biology
  • Genetics
  • Cancer Research

Background:

  • The deleted in colorectal cancer (DCC) gene is frequently altered in colorectal tumors.
  • DCC inactivation is also observed in other cancers, including pancreatic, stomach, breast, prostate, brain, and leukemias.

Purpose of the Study:

  • To characterize the complementary DNAs (cDNAs) and protein products of the DCC gene.
  • To investigate DCC expression patterns in normal and cancerous tissues.

Main Methods:

  • cDNA sequencing from human fetal brain and neuroblastoma cells.
  • Analysis of alternative splicing in mouse tissues.
  • Immunoblotting and immunoprecipitation using DCC-specific antisera.
  • Tunicamycin treatment to assess glycosylation.

Main Results:

  • The DCC gene encodes a transmembrane protein of 1447 amino acids with distinct extracellular and cytoplasmic domains.
  • Two alternative splice sites were identified in DCC cDNAs.
  • DCC transcripts are present at low levels in adult mouse tissues, with alternative splicing observed.
  • DCC protein species (175-190 kDa) are glycoproteins, with highest expression in brain and neural crest cells.
  • DCC expression is markedly reduced or absent in most cancer cell lines studied.

Conclusions:

  • The DCC gene encodes multiple related glycoprotein species.
  • DCC glycoproteins are expressed at low levels in normal adult tissues.
  • Reduced or absent DCC expression in cancer cell lines may result from genetic inactivation.

Related Concept Videos

RNA Splicing01:32

RNA Splicing

Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
Alternative RNA Splicing02:18

Alternative RNA Splicing

Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
Exon Recombination02:32

Exon Recombination

The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes. 
Exon shuffling follows “splice frame rules.” Each exon has three reading...
Abnormal Proliferation02:23

Abnormal Proliferation

Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter...
Loss of Tumor Suppressor Gene Functions01:12

Loss of Tumor Suppressor Gene Functions

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
Loss of Tumor Suppressor Gene Functions01:12

Loss of Tumor Suppressor Gene Functions

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...