Gene Dmel\Fas1
| General Information | ||||
|---|---|---|---|---|
| Symbol | Dmel\Fas1 | Species | D. melanogaster | |
| Name | Fasciclin 1 | Annotation symbol | CG6588 | |
| Feature type | protein_coding_gene | FlyBase ID | FBgn0000634 | |
| Created / Updated | 2003-12-01/2008-06-17 | |||
| Genomic Location | ||||
| Chromosome (arm) | 3R | Recombination map | ||
| Cytogenetic map | 89D5-89D6 | Sequence location | 3R:12,450,948..12,465,493 [+] | |
| Map ( GBrowse ) |
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Summary Information
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Automatically generated summary
See sections below for more information | The gene Fasciclin 1 is referred to in FlyBase by the symbol Fas1 (CG6588, FBgn0000634). It has the cytological map location 89D5-89D6. Its sequence location is 3R:12450948..12465493. Its molecular function is described as cell adhesion molecule binding. It is involved in the biological processes: neuron recognition; axon guidance; calcium-independent cell-cell adhesion; homophilic cell adhesion; neuron adhesion. 22 alleles are reported. No phenotypic data is available. It has 6 annotated transcripts and 6 annotated polypeptides. | |||
| External Summaries | ||||
Phenotypic Description from the Red Book (Lindsley & Zimm 1992)
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| Gene/Allele symbols may differ from current usage | Fas1: Fasciclin I
Expression confined to neurons. In 12-14 h embryos
high levels of fasciclin I are detectable in two commissural
axon bundles (fascicles) per segment, a thick one in the posterior commissure and a thin one in the anterior commissure.
In addition high expression is seen in two clusters of neuronal cell bodies per hemisegment as well as in the intersegmental and segmental nerve axons. Finally, fasciclin I is
detected on the surface of all peripheral neurons. Postulated
to be involved in neuron recognition during growth cone guidance. Flies deficient in FasI function are fully viable and
CNS development apparently is normal.
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Detailed Mapping Data
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| FlyBase Computed Cytological Location | ||||
Cytogenetic map Evidence for location 89D5-89D6
Limits computationally determined from genome sequence between P{lacW}CSN5L4032 and P{EP}MESK4EP1015
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| Experimentally Determined Cytological Location | ||||
Cytogenetic map Notes References 89E1-89E2 (determined by in situ hybridisation) 89D (determined by in situ hybridisation)
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| Experimentally Determined Recombination Data | ||||
| Location | ||||
| Left of (cM) | ||||
| Right of (cM) | ||||
| Notes | ||||
| Molecular Map Data | ||||
Gene Order (in direction of increasing cytology)
References In direction of increasing cytology: Fas1+ nonA-l+ Cctγ+ CG14906- CG31217- CG31217- Ubx- bxd- Glut3+ abd-A- iab-4+ CG10349+ Abd-B- Actn3- Ahcy89E- In direction of increasing cytology: Fas1? nonA-l? Cctγ? Ubx? Gene Order (overall orientation not stated) References | ||||
Gene Model & Products
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Please see the
GBrowse view of
Dmel\Fas1
for information on other features
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| Comments on Gene Model | ||||
Transcript Data
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| Annotated Transcripts | ||||
Name FlyBase ID RefSeq ID Length (nt) Associated CDS (aa) FBtr0112803
3106
662 FBtr0300036
3279
624 FBtr0300037
3315
636 | ||||
| Additional Transcript Data & Comments | ||||
| Reported size (kB) | 5.2, 5.0, 4.2, 4.0, 3.2, 3.0 (northern blot) 3.0 (longest cDNA) | |||
| Comments | This minor transcript is expressed at high levels in Schneider 1 cells. This major transcript is expressed at high levels in Schneider 1 cells. PCR analysis shows that Fas1 transcripts can vary by 3 or 6 amino acids through the inclusion or exclusion of two 9 bp microexons (exons 8 and 9). Type I transcripts contain neither microexon, type II transcripts contain exon 8, and type III transcripts contain both exone expressed in isolated 10-13 hr ventral nerve cords. Its expression pattern suggests that the 3.0 kb Fas1 transcript can exist in type I and type II forms.
e expressed in isolated 10-13 hr ventral nerve cords. Its expression pattern suggests that the 3.0 kb Fas1 transcript can exist in type I and type II forms. This major transcript is expressed at high levels in Schneider 1 cells. PCR analysis shows that Fas1 transcripts can vary by 3 or 6 amino acids through the inclusion or exclusion of two 9 bp microexons (exons 8 and 9). Type I transcripts contain neither microexon, type II transcripts contain exon 8, and type III transcripts contain both exons 8 and 9. Type I is dominant in embryogenesis, type II is expressed at 9-15 hours of embryogenesis, and type III is expressed at low levels in embryogenesis with a peak at 9-15 hours. All 3 types
re expressed in isolated 10-13 hr ventral nerve cords. Its expression pattern suggests that the 5.0 kb Fas1 transcript can exist in type I form. The 3.0 and 5.0 kb major Fas1 transcripts, and the 3.2, 4.0, 4.2, and 5.2 kb minor Fas1 transcripts encode the same polypeptide, and differ in the length of the 3\\' untranslated region. A low level of heterogeneity within each transcript size class is seen, however, as a result of the use of two alternate micro-exons (exons 8 and 9), which give rise to polypeptides differing from the shortest Fas1 isoform by 3 or 6 amino acids. | |||
| External Data | ||||
| Crossreferences | ||||
Polypeptide Data
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| Annotated Polypeptides | ||||
Name FlyBase ID
Predicted MW (kD)
Length (aa)
Theoretical pI
RefSeq ID
GenBank protein
FBpp0111715
73.7
662
7.53
FBpp0289313
69.5
624
6.91
FBpp0289314
70.9
636
6.63
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| Additional Polypeptide Data & Comments | ||||
| Reported size (kD) | 72 (kD observed) 652 (aa); 70 (kD predicted) | |||
| Comments | Fas1 is an extrinsic membrane protein, composed of 4 homologous domains of 150 aa each. In Schneider 1 cells, Fas1 was found to be tightly associated with the lipid bilayer by a phosphotidylinositol lipid moiety. The proportion of membrane bound to soluble Fas1 was assayed during embryogenesis. The amount of membrane-bound, phosphatidylinositol-linked Fas1 was higher from blastoderm to early gastrulation stages. During germ band extension and retraction, the amount of soluble Fas1 was 3 times higher than membrane-bound Fas1. Later, as Fas1 expression became restricted to the nervous system and a few other tissues, the phosphatidylinositol linked form was once again the predominant form. | |||
| External Data | ||||
| Linkouts | PANTHER
- Protein classification by function, families, and pathways
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| Crossreferences | InterPro
domains - A database of protein families, domains, and functional sites
• Beta-Ig-H3/fasciclin (IPR000782)
PDB
- Protein Data Bank. An information portal to biological macromolecular structures
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Sequences Consistent with the Gene Model
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| DDBJ
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EMBL / GenBank | DNA sequence Protein sequence Name | |||
