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J. Biol. Chem., Vol. 277, Issue 21, 18494-18500, May 24, 2002

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Elovl1 and p55Cdc Genes Are Localized in a Tail-to-Tail Array and Are Co-expressed in Proliferating Cells^*

Abolfazl Asadi, Johanna Jörgensen, and Anders Jacobsson

From the Wenner-Gren Institute, The Arrhenius Laboratories F3, Stockholm University, SE-106 91 Stockholm, Sweden

Received for publication, December 3, 2001, and in revised form, February 25, 2002

	ABSTRACT

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Elovl1 is a ubiquitously expressed gene, the product of which belongs to a highly conserved family of microsomal enzymes, which are involved in the formation of very long chain fatty acids and sphingolipids in yeast to man. To elucidate the structure and regulation of the Elovl gene we have isolated a lambda phage genomic DNA clone containing the entire mouse gene and found that Elovl1 consists of eight exons that are dispersed over 5.4 kb of genomic sequence. Interestingly, sequencing of the lambda clone to completion revealed that the insert contained a segment of the cell cycle gene p55Cdc directed in the opposite orientation. The genes are very tightly linked so that the 3'-end of the long mRNA species are complementary over a short stretch of nucleotides. Although both Elovl1 and p55Cdc are highly conserved genes, a BLAST search implies that the tail-to-tail arrangement has evolved in vertebrates. Despite the non-similar expression pattern in different tissues, mRNA analysis of the two genes disclosed simultaneous transcription during a proliferation-differentiation transition state, which suggests that the two genes may be regulated through a common bi-directional transcription mechanism under specific conditions.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Very long chain fatty acids (VLCFA)¹ have been recognized as structural components in a variety of fat molecules such as glycerophospholipids, sphingolipids, and wax- and sterol esters. Depending on their chain length and degree of unsaturation, they contribute to the fluidity and other physical and chemical properties of the membrane. VLCFA are found in virtually all cells and are major constituents of the brain, skin and testis. For example, the brain contains high amounts of VLCFA consisting of 24 or more carbons, which are required for normal brain myelination (1). VLCFA are also needed in the synthesis of ceramides, which are necessary for the formation and function of the permeability layer of the skin. The ceramides, together with free VLCFA, comprise more than 50% of the fatty acids found in the epidermis, the outermost layer of the skin, which is the highest amount present in any mammalian tissue (2).

Synthesis of VLCFA is performed in the endoplasmic reticulum and in mitochondria by membrane-bound enzymes; the former is more prominent (3). Elovl1² (4) is a highly conserved gene that shows extensive sequence identity to the earlier identified gene Elovl3 (5, 6). Both are members of a recently identified mammalian gene family whose products have been shown to be involved in the formation of VLCFA and sphingolipids (4, 7-13).

Elovl1 is expressed in all tissues tested and the enzyme is believed to elongate very long fatty acids up to C₂₆ (4). Especially high levels of expression are found in stomach, lung, kidney, skin, and intestine (4), which suggests that ELOVL1 may be important for developing a proper barrier in epithelial cells and skin. In addition, ELOVL1 has also been suggested to be a crucial enzyme involved in the formation of myelin in the central nervous system in mouse (4).

Although the Elovl1 mRNA sequence has been identified, very little is known about the genetic nature of mammalian fatty acid chain elongation enzymes. To scrutinize the genomic background and regulation of Elovl1 in greater detail we have isolated a lambda phage genomic DNA clone containing the entire mouse Elovl1 gene. Surprisingly, we found that the Elovl1 gene is linked to the gene coding for the cell cycle protein p55Cdc (14) in a bi-directional manner. Despite the fact that both genes are very tightly linked and expressed in all cell types at some point, our findings indicate a complex co-regulation during the cell cycle. Even more surprising is that a similar tail-to-tail arrangement was also found for the Elovl3 gene and the homeobox gene Pitx3 (6). It is therefore intriguing that two closely related genes from the same gene family are both juxtaposed with two completely unrelated genes in a tail-to-tail arrangement.

	MATERIALS AND METHODS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Mouse Elovl1 Genomic Cloning-- Genomic clones of Elovl1 were isolated by plaque hybridization of a commercial mouse 129 strain liver genomic DNA library in the Lambda FIX II vector (Stratagene, cat. no. 946308) with a ³²P-labeled probe corresponding to 0.92 kb from the 5'-end of the Elovl1 cDNA (GenBank^TM accession no. AF170907). Hybridization was carried out overnight at 45 °C in 50% formamide, 5× SSC, 5× Denhardt's solution, 50 mM sodium phosphate, pH 6.5, 0.5% SDS, and 100 µg/ml degraded herring sperm DNA. The membranes were first washed twice for 15 min at room temperature in 2× SSC, 0.1% SDS, and a high stringency wash was then performed at 55 °C in 0.1× SSC, 0.1% SDS for 15-30 min. Screening of ~1.5 × 10⁶ plaques yielded one positive recombinant, which was isolated by two additional rounds of plaque purification. Phage DNA was prepared on a large scale by the polyethylene glycol precipitation method according to Ref. 15. Restriction fragments generated by various combinations of restriction enzymes were analyzed by Southern blotting.

Mouse p55Cdc cDNA Cloning-- For sequencing of a full-length mouse p55Cdc cDNA, we combined the sequences from three EST clones (accession nos. AI327152, AA497914, and AA537091) obtained from the I.M.A.G.E. Consortium and a 735-bp RT-PCR (Promega, cat. no. A1250) product obtained from mouse liver total RNA covering the 3'-end of p55Cdc mRNA. At least two independent PCR products were sequenced to check that no amplification errors occurred. RT-PCR experiments were performed using primer 5'-GATCAAGGAGGGCAACTACC-3' for the 5'-end and primer 5'-GCTTTTTCCCGCTACGCCGA-3' for the 3'-end. The PCR products were subcloned into pCR-XL-TOPO vector (Invitrogen, cat. no. K4700-10) and sequenced.

DNA Sequencing and Sequence Analysis-- Using recombinant phage DNA as a template, the genomic insert was sequenced by the primer walking strategy. Sequencing was performed with an ABI 373A automatic DNA sequencer (Applied Biosystems) on reactions prepared by the dye-termination method, using the ABI Prisms Dye Terminator Cycle Sequencing Ready Reaction kit (PerkinElmer Life Sciences, Applied Biosystems, cat. no. 4303149). The sequence information was compiled and analyzed with the use of the University of Wisconsin Genetics Computer Group software (16). The complete nucleotide sequence of a 6034-bp genomic fragment and the p55Cdc cDNA sequence has been deposited in GenBank^TM (accession nos. AF322919 and AF312208).

RNA Isolation, Northern Blotting, and DNA Probes-- Total RNA was isolated using the ULTRASPEC^TM RNA Isolation System (Biotecx) from the different tissues of a 6-week-old NMRI male mouse kept at room temperature and from the brown adipose tissue of another sibling male mouse that was cold-exposed at 4 °C for 3 days. Northern blotting and hybridization were performed as previously described (5).

The DNA probes used were the Elovl1 ORF probe (a 923-bp fragment corresponding to nt 104-1027 in the Elovl1 cDNA) and the p55Cdc probe (a 1.75-kb fragment corresponding to full-length cDNA). The probes were labeled with [-³²P]dCTP using a random-primed DNA labeling kit (Roche Molecular Biochemicals).

RT-PCR Transcription Analysis-- DNase-treated total RNA (1.5 µg from brown fat, kidney, heart, and liver) was reverse-transcribed and amplified in one step using a Promega Access RT-PCR System kit (cat. no. A1250). The PCR reaction was carried out with the primers: forward, 5'-CGGGAAACCACTGAGATTGT-3' and reverse, 5'-ATCTTCCTTATGTCCCAGCA-3', for the Elovl1 amplification; and the primers forward, 5'-CTCAGCGGCAAACCTCAGAA-3' and reverse, 5'-ACTGGTTCCTCCTCCTGTTG-3' for p55Cdc amplification. The following cycle parameters were used: 48 °C for 45 min, 94 °C for 2 min (RT), 94 °C for 30 s, 60 °C for 1 min, 68 °C for 2 min (40 cycles), 68 °C for 7 min (PCR), 4 °C soak. The PCR products were electrophoresed in a 2% agarose gel in 0.5× Tris borate/EDTA buffer and photographed.

PCR Analysis of the Elovl1/p55Cdc Gene Linkage-- For PCR analysis of the Elovl1/p55Cdc gene linkage genomic C57BL/6 mouse DNA was used as template. The PCR reaction was carried out with primers 5'-GTCAGAATGGGCAGGCAGCA-3', complementary to mouse Elovl1 genomic sequence 5008-5027, and 5'-GGGGCCTGTCTGAGTGCTGTGGAT-3', complementary to p55Cdc mouse mRNA sequence 1287-1310.

DNA Extraction and Southern Blotting-- Genomic DNA was prepared from mouse tails by the simplified mammalian DNA isolation procedure published by Laird et al. (17). Tail biopsies were collected from 3-week-old mice of the C57BL/6J strain and used directly for DNA isolation.

Digested DNA was separated on an 0.8% agarose gel and transferred to a Hybond N+ membrane (Amersham Biosciences) according to standard procedures (15). Hybridization and washing conditions were identical to those used for library screening, except that the second wash was carried out under low-stringency conditions (15 min at 40 °C in 0.5× SSC, 0.1% SDS). The radiolabel was detected by exposure to DuPont Cronex x-ray films with an intensifying screen at 80 °C.

Cell Culture-- HIB-1B cells, provided by Dr. B. Spiegelman (Boston, MA), were grown in pre-adipocyte medium (PAM), i.e. Dulbecco's modified Eagle's medium, supplemented with 2 mM glutamine and 10% heat-inactivated fetal calf serum (18). Cells were induced to differentiate in adipocyte medium (AM) by the addition of 20 nM insulin and 1 nM triiodothyronine. At this stage, the cells were allowed to become confluent without a change of medium for up to 3 days (19).

	RESULTS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Isolation of a Mouse Elovl1 Genomic Clone-- A 129 SvJ mouse genomic DNA library was screened with an Elovl1 cDNA probe (4) that resulted in a clone containing a 17-kb fragment. By subsequent hybridization with probes specific for the 5'- and 3'-ends of the Elovl1 cDNA, the fragment was identified as covering the entire Elovl1 gene. The nucleotide sequence was determined by primer walking strategy directly from the phage DNA.

Organization of the Elovl1 Gene-- The Elovl1 gene spans ~5.4 kb of genomic DNA and is composed of eight exons (Fig. 1A). The exons range in size from 58 to 720 bp and the introns range from 77 to 2285 bp. The sequences at the exon/intron junctions are reported in Table I. As indicated, the splice junctions of the seven intervening introns are well conserved and follow the gt-ag rule (20) and score highly in terms of the derived consensus sequences at these sites (21). In contrast to our sequencing data obtained from a full-length Elovl1 cDNA (4), we were unable to identify a genomic sequence containing the first 41 bp previously described within the cDNA fragment. However, our genomic sequence does not contain a conserved splice acceptor site, which would have supported the existence of an extra 5'-exon. Furthermore, we have not been able to retrieve any EST sequence containing the extra 41 bp. This difference is presumably due to a cloning artifact of the mouse cDNA because the human gene (GenBank^TM accession no. AL139289) also lacks the corresponding sequence. The translation initiation codon (ATG) is located in the second exon, and the protein coding sequence stretches into the eighth exon. The proximal promoter sequence does not contain a TATA-box consensus site. Instead, there are several short interspersed GC-rich elements in the close vicinity of the transcription start site. The polyadenylation signal earlier described by Tvrdik et al. (4) is located within the eighth exon at 5064-5070 bp.

View larger version (13K): [in this window] [in a new window]   Fig. 1.   Schematic representation of the Elovl1 and p55Cdc loci. A, exon/intron structure and orientation of Elovl1 and p55Cdc. Exons are numbered and indicated by boxes on the transcribed DNA strand. Protein-coding regions within the mouse genomic sequence are solid, 5' and 3' untranslated regions are hatched and correspond to the Elovl1 and p55Cdc mRNA sequence (previously published by us (4) and in this paper, respectively) (GenBankTM accession nos. AF170907 and AF312208). Polyadenylation signal consensus sequences (pA) are marked by small vertical arrows. Numbers above the sketch refer to nucleotide positions in GenBankTM accession no. AF322919 of the mouse genomic sequence. One EST cDNA fragment (GenBankTM accession no. AA718173/BM445297) corresponding to the 3'-end of mouse Elovl1 mRNA is positioned according to its homology with the genomic DNA. The hatched intron sequence and the solid white exons within the p55Cdc gene correspond to data obtained from the rat gene (14) (GenBankTM accession no. AF052695). B, PCR analysis of 3' Elovl1/p55Cdc genomic mouse DNA. Genomic DNA (gDNA; 1.5 µg) was amplified with mouse sequence-specific primers as described under "Materials and Methods" and shown in A. M, 1-kb Plus DNA Ladder molecular weight marker (Invitrogen).

Elovl1 Is a Single Copy Gene-- To verify if Elovl1 is a single copy gene we performed a Southern blot analysis of mouse DNA. As shown in Fig. 2, following digestion with BglI, SacI, and XbaI, the mouse Elovl1 ORF probe only strongly hybridized to genomic fragments that were of the predicted size, suggesting that Elovl1 is a single copy gene in the mouse genome.

View larger version (57K): [in this window] [in a new window]   Fig. 2.   Detection of the Elovl1 gene in mouse genomic DNA. Southern blot analysis was performed with 10 µg/lane of mouse genomic DNA digested with the indicated restriction enzymes: B, BglI; S, SacI; X, XbaI. The blot was hybridized to the Elovl1 ORF probe and washed as described under "Materials and Methods."

Elovl1 Is Tightly Linked to p55Cdc-- Sequencing of the untranscribed flanking regions of the Elovl1 gene revealed that the cloned insert contained part of yet another gene closely linked to the 3'-end of the Elovl1 gene. A BLAST search identified the sequence as corresponding to the cell cycle gene p55Cdc (Fig. 1A) (14). p55Cdc is a mammalian homolog of a family of cell cycle proteins from widely divergent species that has been implicated in cell cycle-regulated ubiquitin-mediated proteolysis (22-25). The p55Cdc gene consists of 10 exons and has been analyzed in detail in rat (GenBank^TM accession no. AF-052695) (14) (Fig. 1A) but not in mouse or man. Our lambda genomic clone covers the last 688 nucleotides of the p55Cdc gene including the last exon and intron and part of exon number 9. The sequence identity between the published genomic rat p55Cdc and the sequence we have determined from our genomic clone is 86% over a total region of 1189 nucleotides.

To confirm the Elovl1/p55Cdc organization in mouse we ran a PCR with mouse genomic DNA as a template. An expected fragment of ~2200 bp was obtained with primers complementary to a sequence within exon 8 of Elovl1 and within the mouse p55Cdc mRNA corresponding to a sequence within exon 8 ~1900 bp into the p55Cdc gene (see below and under "Materials and Methods") (Fig. 1, A and B). Sequence analysis of the DNA fragment confirmed the nucleotide identity as mouse Elovl1/p55Cdc.

Although both Elovl1 and p55Cdc are highly conserved genes, a BLAST search suggests that the tail-to-tail arrangement has evolved in vertebrates (Table II). Linkage data from the WICGR Mouse RH Gene Map Release Data suggests that this region of human chromosome 1 has its equivalence on mouse chromosome 4. 

Identification of Full-length Mouse p55Cdc cDNA Sequence-- The mRNA for p55Cdc has been sequenced for rat and human (23) but not for mouse. To confirm the p55Cdc sequence, we compared the genomic p55Cdc sequence from mouse to the EST data base and found several highly similar nucleotide sequences. Three clones (accession nos. AI327152, AA497914, and AA537091) were acquired from the I.M.A.G.E. Consortium. The full-length cDNA sequence was obtained by sequencing the overlap of these three clones and a 735-bp RT-PCR product covering the 3'-end of p55Cdc mRNA. The nucleotide sequence is shown in Fig. 3.

View larger version (46K): [in this window] [in a new window]   Fig. 3.   Nucleotide sequences of p55Cdc cDNA. Indirect amino acid sequences of the corresponding p55Cdc polypeptide were shown below the open reading frame. Polyadenylation signal consensus sequence is underlined. Sequence data have been deposited under the GenBankTM accession no. AF312208.

Sequence identity between the cDNA sequence and the sequence we determined from our genomic clone was 100% over a total region of 243 nucleotides. The sequence identity between the published rat cDNA p55Cdc and the mouse cDNA was 91%.

Overlapping 3'-Ends of a Long Elovl1 and p55Cdc mRNA Species-- Elovl1 and p55Cdc are oriented in a tail-to-tail manner in a remarkably tight linkage. In fact, there exists a submitted EST sequence from the WashU-HHMI Mouse EST Project with accession number AA718173 corresponding to a Elovl1 mRNA from mammary gland that appears to overlap the transcribed p55Cdc mRNA with 16 nucleotides. We acquired the clone and verified the complete nucleotide sequence versus our genomic clone over a total region of 560 nucleotides. From our sequence data, we were able to identify 37 additional nucleotides, which were complementary to exon 10 of the p55Cdc gene, as well as a 50-bp-long poly(A) tail (GenBank^TM accession no. BM445297). These results show that there is a total overlap of 53 nucleotides in the two transcripts (Figs. 1A and 4C). Because we have not detected more than one mRNA species on our Northern blots (see Fig. 6), this is probably not a major cleavage site of Elovl1 transcription.

View larger version (18K): [in this window] [in a new window]   Fig. 4.   Nucleotide sequence alignment of one Elovl1 EST clone obtained from mammary gland with genomic DNA (GenBankTM accession no. AF322919) and 3'-end of p55Cdc cDNA. A, 3'-end cDNA sequences corresponding to primary mRNA species cleaved immediately downstream of the polyadenylation signal (AATTAAA) in Elovl1 (AF170907). B, cDNA sequences corresponding to overlapping transcripts and predicted polyadenylation signal for the long Elovl1 transcript obtained from mammary gland (GenBankTM accession no. BM445297). AF312208, p55Cdc cDNA GenBankTM accession no.

To confirm the presence of overlapping mRNA species in different tissues, we performed RT-PCR on total RNA from brown adipose tissue, kidney, heart, and lung with primers corresponding to the 3'-untranslated region of the long Elovl1 mRNA from mammary gland (GenBank^TM accession no. AA718173). As shown in Fig. 5A, we amplified the anticipated 307 bp product (primers from nt 5075 to 5094 and nt 5363 to 5382 in the genomic clone) in brown adipose tissue, kidney, heart, and lung, confirming that such Elovl1 transcripts exist that overlap p55Cdc by 53 bp (Fig. 4C). In contrast, we were unable to amplify a specific fragment within the same tissues with primers specific for p55Cdc (primers from nt 516 to 535 and nt 1234 to 1253 in the cDNA clone) (Fig. 5B).

View larger version (38K): [in this window] [in a new window]   Fig. 5.   PCR analysis of 3' Elovl1 mRNA (A) and p55Cdc mRNA (B) expression in mouse tissues. DNase-treated total RNA (1.5 µg) was reverse-transcribed and amplified. Lane 1, brown fat; lane 2, kidney; lane 3, heart; lane 4, liver; lane 5, p55Cdc cDNA. M, 1-kb Plus DNA Ladder molecular weight marker (Invitrogen).

Contrasting Expression of Elovl1 and p55Cdc in Different Mouse Tissues-- The ELOVL1 protein is involved in the formation of membrane lipids and earlier results revealed that Elovl1 was ubiquitously expressed (4). The p55Cdc is highly expressed in proliferating but not in differentiated or growth-arrested cells (24).

To verify the Elovl1 and p55Cdc expression, we first compared the mRNA levels within different tissues. As seen in Fig. 6, the expression pattern in different tissues was dissimilar for the two genes. In agreement with our earlier results, the Elovl1 expression was diversified in different mouse tissues, with the highest steady-state mRNA levels in stomach, lung, kidney, skin, intestine, and some specific brain tissues, whereas white fat, liver, spleen, brown fat, heart, and muscle showed moderate Elovl1 expression. Only a very weak Elovl1 mRNA signal was found in the testis.

View larger version (44K): [in this window] [in a new window]   Fig. 6.   Elovl1 and p55Cdc mRNA levels in mouse tissues. Northern blot analyses were performed with 10 µg of total RNA isolated from the tissues indicated. BAT, 4 °C, refers to RNA isolated from the brown adipose tissue of a mouse exposed to 4 °C for 3 days. All other RNA samples were isolated from animals kept at thermoneutral temperature (28 °C). WAT, white adipose tissue; SK. MUSCLE, skeletal muscle. The membranes were probed with 32P-labeled cDNA fragments corresponding to open reading frames of Elovl1 and p55Cdc, respectively and subsequently exposed to DuPont Cronex x-ray films for up to 1 week. The position of the ribosomal 18 S RNA is indicated on the right.

In contrast, the highest level of p55Cdc mRNA was found in testis, whereas spleen and intestine showed moderate expression. Low or undetectable amounts of p55Cdc mRNA were obtained from fat tissue, liver, brain, lung, stomach, muscle tissue, and skin.

Elovl1 and p55Cdc Expression Is Affected in a Similar Way During Differentiation of HIB-1B Cells-- To see if the pattern of mRNA levels for the two genes was synchronously affected during cell growth, we analyzed the expression pattern in a brown fat cell line, HIB-1B, during a proliferative stage and when cells were induced to differentiate. These cells, which are derived from a brown fat hibernoma, are known to differentiate in culture when they reach confluence and are subsequently exposed to a differentiation medium (18). During the preconfluent stage, the cells showed the highest level of expression of both genes (Fig. 7). After confluence, the cells showed decreased levels of both Elovl1 and p55Cdc mRNA with time, even if the culture medium was not changed to differentiation medium. This indicates that, although the genes were shown to be independently regulated in a tissue-specific manner, during a specific phase of development, certain cells may have a synchronized expression of Elovl1 and p55Cdc mRNA.

View larger version (66K): [in this window] [in a new window]   Fig. 7.   Elovl1 and p55Cdc mRNA levels in cultured HIB-1B cells. Northern blot analyses were performed with 10 µg of total RNA isolated from cells cultured in pre-adipocyte medium (PAM) until confluence (PAM, 0), after confluence for 2 days in pre-adipocyte medium (PAM, 2), or for 2 or 3 days in adipocyte medium (AM, 2 and 3).

	DISCUSSION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Elovl1 is a highly conserved gene and a member of a recently recognized mammalian gene family whose products have been indicated as being involved in the formation of very long chain fatty acids and sphingolipids (4)

We have isolated here a lambda phage genomic DNA clone containing the entire mouse Elovl1 gene. Although the length of the gene, as well as the transcript, is relatively similar to the closely related gene Elovl3, the exon-intron structure is markedly different (8 exons versus 4 exons) (6). Because the encoded polypeptides are very similar both in size and sequence, there is no obvious explanation for these structural differences.

Surprisingly, sequencing of the lambda clone revealed that the insert contained the 3' part of the newly identified cell cycle gene p55Cdc (14) in the opposite orientation. The genes are very tightly linked, so the 3'-ends of their long mRNA species are complementary over a short stretch of nucleotides.

Despite the fact that overlapping genes are rare events in eukaryotes (26-28), a similar tail-to-tail arrangement was also found for the Elovl3 gene and the homeobox gene Pitx3 (6). Except for homologous genes that may have arisen by gene duplication, adjacent genes are normally separated by tens to hundreds of kilobases within the mammalian genome. It is therefore intriguing that two closely related genes from the same gene family are both juxtaposed with two completely unrelated genes within an 8-9-kb stretch in a tail-to-tail arrangement.

The ELOVL1 protein has been identified as a fatty acid elongase, which elongates VLCFAs up to 26 carbon atoms (4). Under normal circumstances, a substantial amount of VLCFA is linked to a long chain sphingoid base sphinganine, forming a ceramide, which constitutes the lipid backbone of sphingomyelin and other sphingolipids. Sphingolipids are essential for cell proliferation. Impaired sphingolipid synthesis leads to cessation of cell growth both in yeast (29) and mammalian cells (30). Concomitantly, p55Cdc is the mammalian homolog to the cell cycle protein CDC20p in yeast (22, 23) and the Fizzy protein in Drosophila (31) and is required for the metaphase-anaphase transition (32). EST sequences corresponding to both mRNAs can be found as early as in the fertilized egg during mouse development. It is therefore probable that the two genes are expressed during the proliferative phase in any cell type.

Obviously, overlapping genes in opposite orientation generate transcripts that could form RNA duplexes if present in the same cell. In particular, several recent reports show that short stretches of double-stranded RNA molecules may serve as a template for specific RNA nuclease activity leading to gene silencing (33-35). Because both Elovl1 and p55Cdc genes exhibit a rather ubiquitous tissue expression pattern at some point, we can therefore not exclude this possibility that a short tail-to-tail sense-antisense structure may serve as a template for specific RNA nuclease activity leading to gene silencing.

Interestingly, there is an identical 9-bp element, CTCAAAAGA, within the 3'-untranslated region of each gene, 124 and 126 bp, respectively, downstream from the sites where the poly(A) tails are added onto each of the genes. We searched the data base for factors that could recognize this element but no such finding occurred.

The promoter of the p55Cdc gene has been analyzed in rat and contains several cell cycle regulatory motifs, which are known to repress constitutive transcription during G₀ and early G₁ phases of the cell cycle (14). In our study, we show that Elovl1 and p55Cdc have a distinct tissue-specific expression. However, in synchronized brown fat cells, we found that the expression of both genes was high during the proliferative phase and decreased upon differentiation of the cells. This is in agreement with p55Cdc being strictly expressed during mitosis. Notably, although Elovl1 is ubiquitously expressed, its expression is also decreased during differentiation of the cells. This may indicate that both genes are under a common regulator(s) during the cell cycle. One could speculate that there are common constitutive factors that keep the Elovl1-p55Cdc locus in a transcriptionally open position but only during a proliferative phase, and in addition to this there are specific cell cycle factors that apply a specific restriction on the p55Cdc gene. However, an understanding of the mechanism of action of this interesting gene interaction must await further knowledge about interacting factors within the Elovl1 gene.

	ACKNOWLEDGEMENTS

We thank Birgitta Leksell for technical assistance and Jan Nedergaard for valuable comments and suggestions during manuscript preparation.

	FOOTNOTES

^* This work was supported by grants from the Swedish Natural Science Research Council.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the GenBank^TM/EBI Data Bank with accession number(s) AF322919, AF312208, and BM445297.

To whom correspondence should be addressed: The Wenner-Gren Institute, The Arrhenius Laboratories F3, Stockholm University, SE-10691 Stockholm, Sweden. Tel.: 46-8-164127; Fax: 46-8-156756; E-mail: anders.jacobsson@wgi.su.se.

Published, JBC Papers in Press, March 12, 2002, DOI 10.1074/jbc.M111503200

² In accordance with the Mouse and Human Nomenclature Committees the assigning symbols for the mouse genes Scc1, Ssc2, and Cig30 are changed to Elovl1, Elovl2, and Elovl3, respectively.

	ABBREVIATIONS

The abbreviations used are: VLCFA, very long chain fatty acids; EST, expressed sequence tag; RT, reverse transcription; ORF, open reading frame; PAM, pre-adipocyte medium; nt, nucleotides..

	REFERENCES

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

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