Circadian (~24-hr) rhythms in Drosophila melanogaster depend upon cyclic expression of the period (per) and timeless (tim) genes, which encode interacting components of the endogenous clock. The per gene has been isolated from other insects and, more recently, a per ortholog was found in mammals where its expression oscillates in a circadian fashion. We report here the complete sequence of a tim gene from another species, Drosophila virilis. TIM is better conserved than the PER protein is between these two species (76 vs. 54% overall amino acid identity), and putative functional domains, such as the PER interaction domains and the nuclear localization signal, are highly conserved. The acidic domain and the cytoplasmic localization domain, however, are within the least conserved regions. In addition, the initiating methionine in the D. virilis gene lies downstream of the proposed translation start for the original D. melanogaster tim cDNA and corresponds to the one used by D. simulans and D. yakuba. Among the most conserved parts of TIM is a region of unknown function near the N terminus. We show here that deletion of a 32 amino acid segment within this region affects rescue of rhythms in arrhythmic tim01 flies. Flies carrying a full-length tim transgene displayed rhythms with ~24-hr periods, indicating that a fully functional clock can be restored in tim01 flies through expression of a tim transgene. Deletion of the segment mentioned above resulted in very long activity rhythms with periods ranging from 30.5 to 48 hr.
CIRCADIAN (~24-hr) rhythms are displayed by virtually all organisms, ranging from cyanobacteria to mammals (Dunlapet al. 1995; Hall 1995). Circadian rhythms, as distinguished from phenomena that are driven solely by cues in the environment, are generated by an internal time-keeping mechanism called the circadian clock. Because the circadian clock is normally synchronized with the environment, models of a circadian system include an input pathway that conveys information about the environment to the clock (Eskin 1979). Cues in the environment, such as light, reset the phase of the clock, thereby synchronizing the ~24-hr endogenous rhythm with the environmental cycle. The mechanism of resetting has been investigated in at least two systems, and in both, the level of a clock component changes in response to light, producing a predictable phase shift (Crosthwaiteet al. 1995; Hunter-Ensoret al. 1996; Leeet al. 1996; Myerset al. 1996; Zenget al. 1996). A circadian system also includes an output pathway that relays temporal information from the clock to other sites, effecting the circadian regulation of different physiological processes and behavioral activities (Eskin 1979).
Genetic analysis of circadian rhythms has identified four genes that encode clock components. These are the timeless (tim) and period (per) genes in Drosophila, and the frequency and white collar-2 (a transcriptional activator) genes in Neurospora (Dunlapet al. 1995; Sehgalet al. 1996; Crosthwaiteet al. 1997). Recently, two mammalian genes that function in the circadian system were isolated. The first, Clock, is the gene affected in a circadian mutant mouse, and it encodes a novel member of the bHLH-PAS family of transcription factors (Kinget al. 1997; Antochet al. 1997). The second is a mammalian ortholog of the per gene (Sunet al. 1997; Teiet al. 1997).
Where characterized, the clock mechanism involves a molecular feedback loop. In Drosophila, RNA and protein levels of the per and tim genes cycle with an ~24-hr period, and the TIM and PER proteins affect expression of their own mRNAs through a feedback mechanism that requires nuclear entry of TIM and PER (Siwickiet al. 1988; Hardinet al. 1990; Zeng et al. 1994, 1996; Vosshallet al. 1994; Sehgalet al. 1995; Hunter-Ensoret al. 1996; Myerset al. 1996). Nuclear localization of TIM and PER is mediated, at least in part, by association of the two proteins with each other through known interaction domains (Vosshallet al. 1994; Gekakiset al. 1995; Saez and Young 1996). The Neurospora frequency gene operates in a similar autoregulatory feedback loop whereby both RNA and protein cycle and the protein inhibits synthesis of its own RNA (Aronsonet al. 1994). Finally, while the role of the mammalian per gene in the circadian system has not yet been established, it is known that levels of its RNA cycle in the suprachiasmatic nuclei and retina. Both these tissues contain endogenous oscillators (Tosini and Menaker 1996; Turek 1996).
A phylogenetic analysis carried out for per from a number of Drosophila species revealed that much of the coding region (approximately one-third) is not conserved (Colotet al. 1988; Thackeray and Kyriacou 1990). The per gene was also isolated from a non-Dipteran species, Antheraea pernyi, the giant silkmoth (Reppertet al. 1994). Although the giant silkmoth per gene is only 39% identical at the amino acid level to the most closely related Drosophila gene, it was able to rescue circadian rhythms in the arrhythmic per01 Drosophila mutant (Levineet al. 1995). Sequences conserved between the insect per genes, particularly those corresponding to the PAS domain, were used to isolate a mammalian per homolog (Teiet al. 1997). The same gene was isolated fortuitously by a group studying transcripts that mapped to human chromosome 17 (Sunet al. 1997). Surprisingly, given the low level of homology between the insect per genes, mammalian per is ~44% homologous to Drosophila per (including identical amino acids as well as conserved and neutral substitutions; Sunet al. 1997). Conserved regions of PER include all known functional domains, including the PAS domain and the cytoplasmic localization domain, both of which also mediate the interaction with TIM (Gekakiset al. 1995; Saez and Young 1996; Huang et al. 1993, 1995).
Since the cloning of the tim gene (Myerset al. 1995), no one has reported the sequence of a tim homolog. We undertook a phylogenetic analysis of tim by isolating and characterizing a tim homolog from D. virilis, and also by sequencing selected regions of a tim homolog from D. hydei. In this report, we present the intron/exon organization of the gene and the conservation profile of the TIM protein. We found that the amino acid sequence of TIM is more highly conserved overall than that of PER from different Drosophila species, and that most functional domains of TIM are conserved. In addition to known functional domains, such as the PER interaction domains and the nuclear localization signal (NLS), the conserved parts of TIM include an additional region that we show here to be important for function. tim transgenes lacking a 32 amino acid sequence from this region showed aberrant rescue of behavioral rhythms in tim01 flies, while a wild-type tim transgene restored completely normal behavior.
MATERIALS AND METHODS
Fly strains: The D. hydei flies were obtained from Carolina Biological Supply Co. (Burlington, NC), and the homozygous yw; Ki Δ2-3 Drosophila strain was kindly provided by Paul Hardin (Texas A&M University, College Station, TX).
Library screening: The genomic library of D. virilis made in λ phage EMBL3 was kindly provided by R. K. Blackman (University of Illinois, Urbana, IL). This genomic library was screened with a 1.5-kb EcoRI fragment, which corresponds to nucleotides 1974–3492 of the D. melanogaster tim cDNA (Myerset al. 1995; EMBL/GenBank accession number U37018). Hybridization was performed under low stringency conditions (37°, 40% formamide, 6× SSPE, 0.5% SDS, 5× Denhardt's solution, and 0.1 mg/ml salmon sperm DNA). Washes were repeated twice at 50° in a 5× SSPE, 0.1% SDS solution. The library screen yielded two recombinant phage clones that were subjected to Southern blot analysis to identify hybridizing restriction fragments. An ~4-kb BamHI fragment that showed strong hybridization to the tim probe was subcloned and sequenced in both directions. To extend this sequence in the 5′ and 3′ directions, we synthesized primers based on the sequence obtained and used these to sequence phage DNA isolated from our λ phage clones.
A recombinant phage clone containing the upstream sequence of the D. melanogaster tim gene was isolated from a genomic library made in EMBL3A (Spradling and Mahowald 1981) as described above, except that more stringent conditions were used for the hybridization.
RT-PCR experiments of D. melanogaster tim RNA: For the RT-PCR experiment, total RNA was isolated from fly heads by homogenizing them in 0.5 ml of buffer (150 mM sodium acetate, 50 mM Tris, pH 9.0, 5 mM EDTA, pH 8.0, 1% SDS containing 1/100th volume diethyl pyrocarbonate) followed by two phenol/chloroform (1:1) extractions and ethanol precipitation. RNA (in 10 mM dNTP mixture, 20 mM DTT, 1× reverse transciptase buffer containing 10 μM random hexamers and 2 units/μl RNasin) was heated at 65° for 5 min and then cooled to 42°. The reaction mixture was incubated with 1 μl of AMV-reverse transcriptase (10 units/μl, Promega, Madison, WI) for 1 hr at 42°, and the enzyme was then inactivated at 65°. Reverse-transcribed cDNA was amplified by PCR (in 2.5 mM MgCl2, 1× PCR buffer, 2 mM dNTP mixture containing 5 pmol of each primer and 1 μl of Promega Taq polymerase) under the following conditions: 95°, 3 min; 30 cycles of 95°, 30 sec, 55°, 30 sec, 72°, 1 min; 72°, 10 min. A pair of specific primers, which amplifies a fragment corresponding to nucleotides 839–1501 of the original tim cDNA sequence (Myerset al. 1995; GenBank accession number U37018) and spans the 32 amino acid sequence (GenBank accession number AF038501; see results), was used to amplify this region from the reverse-transcribed cDNA and from the original 5′ tim cDNA clone.
3′ RACE: For the 3′ RACE experiment, total RNA was isolated and the reverse transcription was done as described above, except that an oligo-dT primer was used (5′-[C]13 AAGC[T]17-3′) and the reaction was carried out at 37°. Reverse-transcribed cDNA was amplified by PCR as described above, with some modifications. During the first round of amplification, a D. virilis-specific primer (5′-TTGGCTGCAGTTGGTCAT-3′; D. virilis tim sequence, GenBank accession numbers AF038502 and AF040096) and a shorter oligo-dT primer (5′-[C]8 AAGC[T]8-3′) were used, and the annealing temperature was 42° for the initial three cycles and 52° for the remaining 47 cycles. An aliquot of this PCR reaction was then reamplified by PCR using a second D. virilis-specific primer internal to the first (5′-ATGCGCAGCAAATGCAGCA-3′; D. virilis tim sequence, GenBank accession numbers AF038502 and AF040096) and the short oligo-dT primer. The conditions were the same as for the first round of amplification, except that the annealing temperature was 52° for all 40 cycles. The amplified fragments were cloned into the pCR2.1 Vector (Invitrogen, San Diego, CA) and sequenced as below.
Isolation of D. hydei tim sequences: Pairs of degenerate primers were used to amplify, by PCR, regions of the tim gene from D. hydei. The primers were designed based on sequences within regions of the tim gene that were highly conserved between D. melanogaster and D. virilis. The primers were 1S (sense primer) (5′-AA(G/A) CCI CA(A/G) CA(T/C) CA(G/A) AA(G/A/) CC-3′), 4S (5′-GA(T/C) CA(G/A) AT(C/T/A) AA(C/T) AA(T/C) TG(T/C) CT-3′), 13S (5′-GA(C/T) ATG GA(A/G) CA(C/T/) AT(C/T/A/) GA(T/C/) AC-3′), 1A (antisense primer; the exact complement of 1S), and 12A (5′-TC(A/G) TA(G/A) TCI GC(T/C) TCC CA(A/G/T/) AT-3′). Advantage KlenTaq polymerase (Clontech Laboratories, Palo Alto, CA) was used to amplify the following D. hydei fragments. The primer pairs (13S, 12A) and 4S, 1A) amplified a fragment corresponding to nucleotides 2127–2749 and 74–1804 of the D. melanogaster tim cDNA (Myerset al. 1995; GenBank accession number U37018), respectively. The primer pair (1S, 12A) amplified an overlapping fragment corresponding to nucleotides 1785–2749 of the D. melanogaster tim cDNA. A pair of specific primers were made based on the D. hydei sequence to amplify a fragment spanning the 1S/1A primer region. PCR amplification using degenerate primers was done (in 1.5 mM MgCl2, 1× PCR buffer, 0.4 mM dNTP mixture containing 2 pmol of each primer and 1 μl of Taq polymerase) under the following conditions: 95°, 3 min; 3 cycles of 95°, 1 min, 42°, 1 min, 72°, 2 min; 50 cycles of 95°, 1 min, 50°, 1 min, 72°, 2 min; 72°, 10 min. PCR amplification using specific primers was done as described above for 30 cycles, except for omitting cycles 2–4 at a lower annealing temperature. Each fragment was cloned into the pCR 2.1 Vector (Invitrogen) and sequenced as described below.
Sequencing and analysis: Sequencing was done at the University of Pennsylvania Sequencing Facility on an automated sequencer (Applied Biosystems, Foster City, CA) using a dyeterminator and thermal cycling method. The Sequencher program (version 3.0; Gene Codes Corporation, Ann Arbor, MI) was used to create the contigs of independent sequencing reactions. The intron/exon structure of the D. virilis gene was predicted based on its consensus 5′ and 3′ splice sites and by comparison with the D. melanogaster tim cDNA sequence (Myerset al. 1995). We used the DSPL, FGENED, and FEXD programs found on the Baylor College of Medicine Genefinder site (http://dot.imgen.bcm.tmc.edu:9331/gene-finder/gf.html) for prediction of intron/exon junctions, and the Gap and BestFit programs in the Genetics Computer Group (GCG) Wisconsin Software package (version 8.0.1-UNIX) was used for pairwise alignments. The PileUp program (GCG) was used to make multiple sequence alignments, and the amino acid sequence similarity plot was generated by the Plot-Similarity program (GCG).
Construction of plasmids: Plasmids for P-element-mediated DNA transformation were generated by fusing ~4.3 kb of sequence upstream of the transcription initiation site of the D. melanogaster tim gene to the D. melanogaster tim cDNA (Myerset al. 1995; see Figure 4 in this paper). Upstream sequences were isolated by screening a genomic library made in EMBL3A (Spradling and Mahowald 1981) with the 5′ region of genomic clone Ec1 (Myerset al. 1995). An ~7 kb SacI-SacI DNA fragment, which contained a SacI-SwaI fragment extending from approximately −4300 to +180 relative to the transcription initiation site, was isolated from the phage clone.
A full-length tim cDNA was generated by piecing together fragments from partial D. melanogaster cDNA clones (35c and 35g; see Myerset al. 1995). Individual fragments were successively cloned into pBluescript: first, a BamHI-ApaI fragment from the 3′ end, then a SacI-BamHI from the 5′ end, followed by the internal BamHI-BamHI fragment. The orientation of the BamHI-BamHI fragment was verified. The resulting cDNA insert extended from nucleotide positions 1–4955 of the original cDNA sequence and had a 3′ alternatively retained intron inserted after position 3555 (Myerset al. 1995; GenBank accession number U37018), but it did not include the additional 32 amino acid sequence reported in this paper (see results). This full-length cDNA was then excised using SacI and KpnI (polylinker sites) and cloned into the pet-17b vector to introduce a SpeI site at the 5′ end.
The ~4.5-kb SacI-SwaI fragment containing the upstream sequence (see above) was substituted for the 180-bp SacI-SwaI fragment in the tim cDNA pet-17b construct. A SpeI-KpnI fragment derived from the resulting construct, which contained the upstream sequence fused to the tim cDNA, was then cloned into the P element vector pCaSper4, which contains a miniwhite gene p(white), thus enabling selection of transgenic flies by eye color. The resulting pCaSper4 construct was called Tim 1. Another pCaSper4 construct (Tim 4) was made, which was identical to Tim 1, except that it also contained the additional 32 amino acid sequence (see Figure 4). Since the 32 amino acid sequence was contained within a unique SphI fragment in the tim gene, the SphI fragment in the Tim 1 construct was replaced with the corresponding fragment from the genomic clone Ec1 (Myerset al. 1995). The resulting construct was called Tim 4.
Production of transgenic strains: These two constructs were introduced into the Drosophila genome by P-element-mediated DNA. Embryo injections were performed using a yw/yw; Ki Δ2-3 strain (Robertsonet al. 1988), and multiple independent lines carrying each of the two transgenes were derived from the progeny of surviving G0 adults. Each transgene was then introduced into a yw tim01 background.
Behavioral assays: Behavioral analysis was done on transgenic flies carrying only the tim transgene [p(white)tim01/tim01], on siblings that carried a wild-type copy of the tim gene (CyO/tim01), on siblings that carried neither the endogenous tim gene nor the transgene (tim01/tim01), and on wild-type flies (yw strain). Locomotor activity rhythms were monitored using the Trikinetics system, and analysis was done exactly as described previously (Sehgalet al. 1994).
Cloning of a tim homolog from D. virilis: We screened a D. virilis genomic library under low stringency conditions using a D. melanogaster tim cDNA probe that corresponds to nucleotides 1974–3492 (Myerset al. 1995). This probe includes the PER interaction domains of the tim gene, which we assumed would be well-conserved because the TIM interaction domains of the per gene are well conserved between D. melanogaster and D. virilis (Colotet al. 1988). Two recombinant phage clones were isolated. An ~4-kb BamHI fragment that strongly hybridized with the tim cDNA probe on Southern blots was subcloned and sequenced. To extend the sequence in the 5′ and 3′ directions, we synthesized primers based on the sequence obtained and used these to sequence phage DNA prepared from our clones.
Both genomic clones lacked sequences corresponding to the 3′ end of the D. melanogaster tim gene, which includes the cytoplasmic localization domain (CLD) of TIM (Saez and Young 1996). Since this was a known functional domain that was reported to be conserved in TIM (Saez and Young 1996), we used a 3′ RACE method to obtain sequences from the 3′ end of the D. virilis tim cDNA. By using a D. virilis-specific primer that overlapped the coding region in the 3′ end of our genomic clone and an oligo-dT primer, we amplified from D. virilis cDNA a fragment that included nucleotides homologous to the C-terminal 149 amino acids of TIM.
Genomic organization of tim homologs: We characterized >4 kb of D. virilis genomic sequence corresponding to the tim gene. The schematic in Figure 1 represents ~4.7 kb of genomic sequence from the D. virilis homolog beginning at a consensus cap site (Cherbas and Cherbas 1993) just upstream of a methionine codon and continuing through a codon corresponding to amino acid 1194 of the D. virilis TIM sequence. The C-terminal, 149 amino acid stretch obtained through the 3′ RACE experiment is also indicated. The total length of the coding region is 4029 bp, from which we predict a protein of 1343 amino acids.
The genomic organization in Figure 1 shows the intron exon structure of tim. The figure shows this organization for the D. virilis tim gene and for part of the D. hydei tim gene, which was subsequently isolated for comparison of specific sequences (see below). Our limited data on the organization of the tim gene in D. melanogaster and D. hydei indicate that, where examined, the position of introns within the gene is conserved. We found that the positions of introns corresponding to introns 2–4 of the D. virilis gene are conserved in D. hydei (see Figure 1). Also, the position of an intron corresponding to intron 1 in the D. virilis gene is conserved in D. melanogaster. The DNA sequence of introns was not conserved (data not shown).
The predicted translation start site in the D. virilis gene corresponds to a methionine downstream of the proposed start site in the D. melanogaster gene (Myerset al. 1995). This finding is consistent with a recent report that this methionine may, in fact, also be the start site in some strains of D. melanogaster as well as in other Drosophila species (Rosatoet al. 1997). A polymorphism identified in the tim gene from certain D. melanogaster strains, as well as from D. simulans and D. yakuba, generates a premature stop codon shortly after the originally proposed site (Rosatoet al. 1997). Use of the downstream start site would shorten the D. melanogaster TIM protein by 23 amino acids.
Conservation profile of the TIM protein: The amino acid similarity plot in Figure 2A shows the level of conservation across the TIM protein. The predicted amino acid sequences of the tim gene from different Drosophila species are aligned in Figure 2B, with domains relevant to our analysis of TIM indicated. We found that TIM is more highly conserved between D. virilis and D. melanogaster than PER is conserved between these two species, with TIM having a 76% overall amino acid identity compared with 54% overall identity for PER. In contrast to the per gene, which has five nonconserved domains interspersed within the relatively conserved portion of its coding region (Colotet al. 1988), the coding region of the tim gene has only two regions of low homology. The stretch of acidic amino acids found in D. melanogaster TIM (Myerset al. 1995) falls within one such region (Figure 2, A and B).
Most of the known functional domains in TIM are highly conserved. The NLS in D. virilis is identical to that in D. melanogaster, except for the conservative change of a glutamate to an aspartate. Relative to D. melanogaster, the PER interaction domains in D. virilis are 80–85% identical at the amino acid level, a level of conservation that is similar to that for the TIM interaction domains of per (Colotet al. 1988; Thackeray and Kyriacou 1990; Saez and Young 1996). The N-terminal region of D. virilis tim also shows a high degree of homology (90% identical) to the D. melanogaster gene although no functional domain of tim has been mapped to this region. Incidentally, a 32 amino acid sequence within this region was lacking in the original tim cDNA (see below). The CLD recently mapped to the C-terminal end of TIM (Saez and Young 1996), while retained, is one of the least conserved regions, having only 56% amino acid identity between D. virilis and D. melanogaster.
Of note is that the single amino acid mutated in the timSL allele of D. melanogaster (Rutilaet al. 1996), which occurs just upstream of the first PER interaction domain, is conserved in D. virilis. This allele contains a missense mutation that converts threonine 494 to an isoleucine. The mutation does not produce a dramatic phenotype by itself (the wild-type rhythm is shortened by ~0.5 hr in homozygous timSL lines), but it suppresses the perl (long period) mutation, shortening the period by 4 hr and also restoring temperature compensation (Rutilaet al. 1996).
Isolation of homologous sequences of the tim gene from D. hydei: Analysis of D. virilis tim provided some interesting revelations about tim structure. Most importantly, perhaps, it revealed that the acidic region in D. melanogaster, which was thought to be similar to activation domains of transcription factors (Myerset al. 1995), was not conserved, and that an additional 32 amino acid sequence was present within a highly conserved region. To determine the extent to which these findings were universally applicable, we amplified specific sequences of the tim gene from yet another Drosophila species D. hydei. The genomic D. hydei sequence analyzed here begins in the middle of exon 2 in the D. virilis gene and extends through most of exon 5 (see Figure 1). Protein-coding sequences within this region are represented in Figure 2B and were included in the profile analysis shown in Figure 2A. The following facts were confirmed by our analysis of the D. hydei sequence: (1) the acidic region is poorly conserved, (2) the region N-terminal to this is very well-conserved and includes the additional 32 amino acids, (3) the PER interaction domains are conserved, and (4) the amino acid mutated in the timSL allele is conserved.
The tim RNA in D. melanogaster contains an additional sequence: The D. virilis TIM sequence contained an extra 32 amino acids within the highly conserved N-terminal region of the protein (see Figure 2, A and B). Note that the D. hydei tim gene also contains the additional 32 amino acids; however, the original D. melanogaster tim cDNA that was characterized lacked this sequence (Myerset al. 1995). To determine whether this sequence was included in a differentially spliced form of the tim RNA, we carried out RT-PCR experiments. We used a pair of specific primers to amplify a fragment spanning the 32 amino acid region from head RNA of D. melanogaster (yw strain) and from the original 5′ tim cDNA clone (Myerset al. 1995). In Figure 3, lanes 1 and 2 (yw 14 and yw 16) show the fragment amplified by RT-PCR from head RNA collected at Zeitgeber times 14 and 16, when tim RNA is expressed at high levels (Sehgalet al. 1995). The RT-PCR product is of the size predicted (758 bp) if the fragment includes the additional 32 amino acids. The PCR product amplified from the tim cDNA clone (Figure 3, lane 3) is ~100 bp smaller than the RT-PCR product, as expected, since this cDNA clone lacks the 32 amino acid sequence. Other experiments in which control genomic fragments were also amplified confirmed that endogenous tim RNA was ~100 bp longer than the tim cDNA (data not shown). Since we failed to amplify a smaller band from head RNA in all experiments, it is unlikely that the 32 amino acid sequence is part of a differentially spliced message. The other possibility is that the shorter version represents a polymorphic form of the tim RNA that occurs in other strains. However, given that the 32 amino acid sequence is found in both D. virilis and D. hydei homologs of tim and that it is important for tim function (see below), we believe that this is unlikely. Thus, we conclude that it is an integral part of the D. melanogaster tim RNA.
A protein of 1389 amino acids was predicted from the original sequence of the Drosophila tim gene (Myerset al. 1995). The predicted size becomes 1421 after including the additional 32 amino acids. Use of the methionine in D. melanogaster corresponding to the translation start we report here for D. virilis would shorten TIM by 23 amino acids (see also Rosatoet al. 1997).
A tim transgene lacking a sequence in the N-terminal conserved region produces aberrant rhythms in tim01 flies: The functional significance of the conserved region containing the extra 32 amino acid sequence was determined through behavioral rescue experiments. Arrhythmic tim01 flies were transformed with a tim transgene that either contained (Tim 4) or lacked (Tim 1) the 32 amino acid sequence. Each transgene construct consisted of a tim cDNA from D. melanogaster, which included a 3′ alternatively retained intron (Myerset al. 1995) placed under the control of ~4.3 kb of sequence upstream of the transcription initiation site in the D. melanogaster tim gene (see materials and methods). Flies carrying either transgene were examined in constant darkness after entrainment in 12 hr: 12 hr light/dark cycles for several days. We evaluated two independent lines of flies carrying the Tim 4 transgene (see Table 1). In each of these lines, a high percentage of individual flies were rhythmic (72%), and the rhythmic individuals displayed wild-type periods. For the Tim 4-1 line, the average period was 23.7 ± 0.58, and for the other line, Tim 4-6, the average period was 23.4 ± 0.74. These periods are comparable to those seen in wild-type flies (see Table 1). As expected, tim01 siblings that lacked the transgene were arrhythmic. In Figure 4B, we show the locomotor activity plot and periodogram for a representative fly from one of these lines, Tim 4-1.
To determine whether the Tim 1 construct could rescue the arrhythmic phenotype, we evaluated four independent lines of tim01 flies carrying this transgene. In three of these lines, 27–40% of individual flies showed rescue of behavioral rhythms, but the periods were long, ranging from 30.5 to 48 hr; individual lines had average periods of 36.8–38.0 hr (see Table 1). In Figure 4B, we show the locomotor activity plot and periodogram for a representative fly from one of these lines, Tim 1-1. In a fourth line (Tim 1-6), only one of the individuals tested was rhythmic (Table 1). As before, flies carrying a wild-type copy of the tim gene (CyO/tim01 siblings or yw flies) were rhythmic with an average period of 23.6 ± 0.52 (see Table 1). The behavioral analysis of the Tim 1 and Tim 4 flies demonstrates that the 32 amino acid sequence in TIM is necessary for restoring wild-type rhythms to tim01 flies.
We report here the characterization of tim homologues from D. virilis and D. hydei. Our data show that the overall conservation of TIM is higher than that of PER. All known functional domains of TIM are highly conserved (>80% amino acid identity), with the exception of the CLD (Saez and Young 1996), which shows only 56% amino acid identity between D. virilis and D. melanogaster. The PER interaction domains in TIM show the same level of conservation as the TIM interaction domains in PER (Colotet al. 1988). We propose that since interaction between the PER and TIM proteins is an integral part of the clock mechanism, there is genetic selection to conserve the interacting domains. While the CLD, as currently defined, is less well conserved, there are regions within this domain that are identical between D. virilis and D. melanogaster (see Figure 2B). We also report an additional highly conserved region close to the N terminus. Deletion of a 32 amino acid sequence within this region affects the function of a tim transgene.
This is the first report of rescue of the arrhythmic tim01 mutant phenotype using a tim transgene. The wild-type tim transgene, Tim 4, gave wild-type rescue (average period of ~24 hr) in a high percentage of individual flies. We also obtained full rescue using a tim construct in which almost all cDNA sequences (up to amino acid 1228) were replaced with corresponding genomic sequences. Full rescue of the tim01 phenotype contrasts with that often reported for the arrhythmic per01 phenotype. Rescue of per01 flies by genomic per constructs has usually resulted in periods that are somewhat longer than wild type. Best results are produced with a 13.2-kb per construct that includes ~4 kb of upstream sequences and generates periods of ~24.7 hr (Citriet al. 1987). However, fusion of a per cDNA to the same upstream sequence generated wild-type periods (average 23.8 in one line), suggesting inefficient processing of the genomic constructs (Citriet al. 1987). As mentioned above, we didn't see any difference in the behavioral rescues effected by a tim cDNA versus a tim genomic construct.
Behavioral analysis of arrhythmic tim01 flies carrying a tim transgene that either included (Tim 4) or excluded (Tim 1) the additional 32 amino acid sequence reported here demonstrated that this sequence is necessary for restoring wild-type rhythms to tim01 flies, and thus is likely to be part of an important functional domain. Deletion of this domain does not prevent rescue, as might occur if the protein were rendered nonfunctional through instability or incorrect folding, but it lengthens circadian period to levels rarely observed before. A high percentage of arrhythmia accompanies the long-period phenotype, which is also true, although to a lesser extent, of the perl phenotype (unpublished observations). It may be the case that long periods are associated with arrhythmia, perhaps because of variable expressivity or low penetrance. Interestingly, when Clock mutant mice are monitored under freerunning conditions, they display long periods that eventually degenerate into arrhythmicity (Vitaternaet al. 1994).
Since tim was only recently isolated, previous structure-function studies focused on per, and it should be noted that mutagenesis of per does not always produce a phenotype. Deletion of the Gly-Thr repeat in PER has no observable effect on activity rhythms (Yuet al. 1987). Other mutations in per, such as those in the pers domain (Baylieset al. 1992), or a 177-bp deletion within another conserved part of per generate short periods (A. Sehgal, unpublished results). Deletion of PER's NLS, on the other hand, lengthens circadian period, but not to the extent reported here for the Tim 1 construct (Baylieset al. 1992). As we learn more about the biochemical activities of these proteins, the function of specific domains and the effects of mutations in these domains will become clear.
Since tim is only the second Drosophila clock gene characterized, the phylogenetic conservation of this gene is encouraging. The per gene was found to be poorly conserved among Drosophila species, and yet the information gleaned from this analysis facilitated the isolation of additional homologs and will likely help the characterization of these homologs. Likewise, we believe that our analysis of tim will be useful for addressing clock mechanisms in other species. The Neurospora frequency gene has also been isolated from other species (Merrow and Dunlap 1994), and the mouse Clock gene appears to be conserved among vertebrates (Kinget al. 1997). Mutations affecting circadian rhythms have now been identified in several other organisms (Ralph and Menaker 1988; Kondoet al. 1994; Millaret al. 1995; Hickset al. 1996), and the near future will likely see the isolation of new clock genes or homologs of those already known.
We would like to thank M. W. Young for communicating unpublished results and Jeffrey Field for comments on the manuscript. This research was supported by U.S. Public Health Service grants 1F32-NS-09919-01 and 1R01-NS-35703-01A1, by funds from the American Cancer Society and National Service Foundation, and in part by a grant from the Pittsburgh Supercomputing Center through the National Institutes of Health National Center for Research Resources grant 2-P41-RR06009.
Communicating editor: J. J. Loros
- Received August 1, 1997.
- Accepted November 3, 1997.
- Copyright © 1998 by the Genetics Society of America