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SPD3_CAEEL
ID   SPD3_CAEEL              Reviewed;         478 AA.
AC   Q9TYY7;
DT   02-DEC-2020, integrated into UniProtKB/Swiss-Prot.
DT   01-MAY-2000, sequence version 1.
DT   03-AUG-2022, entry version 95.
DE   RecName: Full=Spindle defective protein 3 {ECO:0000312|WormBase:H34C03.1};
GN   Name=spd-3 {ECO:0000303|PubMed:9649522, ECO:0000312|WormBase:H34C03.1};
GN   ORFNames=H34C03.1 {ECO:0000312|WormBase:H34C03.1};
OS   Caenorhabditis elegans.
OC   Eukaryota; Metazoa; Ecdysozoa; Nematoda; Chromadorea; Rhabditida;
OC   Rhabditina; Rhabditomorpha; Rhabditoidea; Rhabditidae; Peloderinae;
OC   Caenorhabditis.
OX   NCBI_TaxID=6239 {ECO:0000312|Proteomes:UP000001940};
RN   [1] {ECO:0000312|Proteomes:UP000001940}
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC   STRAIN=Bristol N2 {ECO:0000312|Proteomes:UP000001940};
RX   PubMed=9851916; DOI=10.1126/science.282.5396.2012;
RG   The C. elegans sequencing consortium;
RT   "Genome sequence of the nematode C. elegans: a platform for investigating
RT   biology.";
RL   Science 282:2012-2018(1998).
RN   [2] {ECO:0000305}
RP   FUNCTION, AND MUTAGENESIS OF LEU-130.
RX   PubMed=9649522; DOI=10.1093/genetics/149.3.1303;
RA   O'Connell K.F., Leys C.M., White J.G.;
RT   "A genetic screen for temperature-sensitive cell-division mutants of
RT   Caenorhabditis elegans.";
RL   Genetics 149:1303-1321(1998).
RN   [3] {ECO:0000305}
RP   FUNCTION, SUBCELLULAR LOCATION, DEVELOPMENTAL STAGE, AND MUTAGENESIS OF
RP   LEU-130.
RX   PubMed=17947426; DOI=10.1534/genetics.107.078386;
RA   Dinkelmann M.V., Zhang H., Skop A.R., White J.G.;
RT   "SPD-3 is required for spindle alignment in Caenorhabditis elegans embryos
RT   and localizes to mitochondria.";
RL   Genetics 177:1609-1620(2007).
RN   [4] {ECO:0000305}
RP   FUNCTION, SUBCELLULAR LOCATION, AND MUTAGENESIS OF 417-HIS--GLU-478.
RX   PubMed=23671424; DOI=10.1371/journal.pgen.1003497;
RA   Labrador L., Barroso C., Lightfoot J., Mueller-Reichert T., Flibotte S.,
RA   Taylor J., Moerman D.G., Villeneuve A.M., Martinez-Perez E.;
RT   "Chromosome movements promoted by the mitochondrial protein SPD-3 are
RT   required for homology search during Caenorhabditis elegans meiosis.";
RL   PLoS Genet. 9:e1003497-e1003497(2013).
CC   -!- FUNCTION: In the first mitotic division in embryos, required for
CC       mitotic spindle alignment and asymmetric cell division (PubMed:9649522,
CC       PubMed:17947426). Required for motor-driven chromosome movement and
CC       homolog searching within the nucleus, and subsequently ensures
CC       homologous chromosome pairing during the prophase stage of meiosis
CC       (PubMed:23671424). {ECO:0000269|PubMed:17947426,
CC       ECO:0000269|PubMed:23671424, ECO:0000269|PubMed:9649522}.
CC   -!- SUBCELLULAR LOCATION: Mitochondrion {ECO:0000269|PubMed:17947426,
CC       ECO:0000269|PubMed:23671424}. Mitochondrion outer membrane
CC       {ECO:0000305|PubMed:17947426}; Multi-pass membrane protein
CC       {ECO:0000255}. Note=Localizes to mitochondria throughout interphase and
CC       mitosis (PubMed:17947426, PubMed:23671424). Localizes to mitochondria
CC       in the pachytene and transition zone regions of the germ cells
CC       (PubMed:23671424). {ECO:0000269|PubMed:17947426,
CC       ECO:0000269|PubMed:23671424}.
CC   -!- DEVELOPMENTAL STAGE: Expressed in embryos.
CC       {ECO:0000269|PubMed:17947426}.
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DR   EMBL; BX284604; CCD65006.1; -; Genomic_DNA.
DR   PIR; T33735; T33735.
DR   RefSeq; NP_501036.1; NM_068635.4.
DR   AlphaFoldDB; Q9TYY7; -.
DR   STRING; 6239.H34C03.1; -.
DR   PaxDb; Q9TYY7; -.
DR   DNASU; 177438; -.
DR   EnsemblMetazoa; H34C03.1.1; H34C03.1.1; WBGene00004954.
DR   GeneID; 177438; -.
DR   KEGG; cel:CELE_H34C03.1; -.
DR   CTD; 177438; -.
DR   WormBase; H34C03.1; CE19499; WBGene00004954; spd-3.
DR   eggNOG; ENOG502TH1Z; Eukaryota.
DR   HOGENOM; CLU_571398_0_0_1; -.
DR   InParanoid; Q9TYY7; -.
DR   OMA; AFYTEEM; -.
DR   OrthoDB; 1237739at2759; -.
DR   Proteomes; UP000001940; Chromosome IV.
DR   Bgee; WBGene00004954; Expressed in germ line (C elegans) and 4 other tissues.
DR   GO; GO:0016021; C:integral component of membrane; IEA:UniProtKB-KW.
DR   GO; GO:0005741; C:mitochondrial outer membrane; IEA:UniProtKB-SubCell.
DR   GO; GO:0005739; C:mitochondrion; IDA:WormBase.
DR   GO; GO:0090220; P:chromosome localization to nuclear envelope involved in homologous chromosome segregation; IMP:UniProtKB.
DR   GO; GO:0009792; P:embryo development ending in birth or egg hatching; IMP:WormBase.
DR   GO; GO:0007129; P:homologous chromosome pairing at meiosis; IMP:UniProtKB.
DR   GO; GO:0000226; P:microtubule cytoskeleton organization; IMP:WormBase.
DR   GO; GO:0040025; P:vulval development; IMP:WormBase.
PE   1: Evidence at protein level;
KW   Membrane; Mitochondrion; Mitochondrion outer membrane; Reference proteome;
KW   Transmembrane; Transmembrane helix.
FT   CHAIN           1..478
FT                   /note="Spindle defective protein 3"
FT                   /id="PRO_0000451404"
FT   TOPO_DOM        1..24
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000305"
FT   TRANSMEM        25..45
FT                   /note="Helical; Name=1"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        46..52
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000305"
FT   TRANSMEM        53..73
FT                   /note="Helical; Name=2"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        74..478
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000305"
FT   MUTAGEN         130
FT                   /note="L->F: In oj35; reduces growth rate and results in
FT                   vulval defects. Produces dead eggs at a restrictive
FT                   temperature. Defective cell division and cytokinesis during
FT                   embryogenesis. Fails to extrude extra maternal pronuclei
FT                   and displays abnormally large polar bodies following
FT                   alignment of the meiotic spindle. Delayed maternal
FT                   pronuclear migration, and paternal pronuclear envelope
FT                   decay near the posterior cortex prior to the pronuclei
FT                   meeting. Defective orientation of the first mitotic spindle
FT                   where the mitotic spindle aligns transversely to the
FT                   anterior-posterior axis. This leads to a mispositioned
FT                   cleavage plane that does not coordinate with the polarity
FT                   axis, and results in a failure of the asymmetric division.
FT                   Astral microtubules are excessive in length as compared to
FT                   wild-type and make contact with the cortex and continue to
FT                   grow along it. Embryonic localization of dnc-1 to the
FT                   centrosomes, along spindle microtubules, and to the plus
FT                   ends of astral microtubules is similar to wild-type, but it
FT                   is enriched at posterior structures resembling P granules.
FT                   In addition, dnc-2 is enriched in the pericentriolar
FT                   region, the mitotic spindle and cytoplasm. 40% increase in
FT                   ATP concentration compared to wild-type. The egg lethality
FT                   and spindle rotation defects are suppressed in a smg-1 RNAi
FT                   mutant background."
FT                   /evidence="ECO:0000269|PubMed:17947426,
FT                   ECO:0000269|PubMed:9649522"
FT   MUTAGEN         417..478
FT                   /note="Missing: In me85; late onset mitotic defects where
FT                   old adults display enlarged nuclei in the mitotic region of
FT                   the germ line. The number of these enlarged nuclei
FT                   increases with age. Defective homologous chromosome pairing
FT                   evident by nuclei with variable degrees of chromosome
FT                   clustering persisting into the pachytene region. Diakinesis
FT                   oocytes do form chiasmata as in wild-type, but in contrast
FT                   to wild-type, the number of chiasmata decreases with age.
FT                   X-chromosomes are frequently involved in non-homologous
FT                   synapses. Increases the number of sun-1-positive foci in
FT                   transition zone nuclei during meiotic prophase, but these
FT                   foci fail to form large aggregates, have reduced movement
FT                   and reduced number of fusion events. Lower basal rate of
FT                   oxygen consumption."
FT                   /evidence="ECO:0000269|PubMed:23671424"
SQ   SEQUENCE   478 AA;  54418 MW;  3874000F2F0D599F CRC64;
     MDQMTVEEKI LEHQELEDGS SSFRWLVSST VIAIGGATVA LYISGKIDWK IPAIEAGLAL
     TAGGTITCGY LWFKKRVKTV RKLILQMNKT RSALRKRRQI FFSISMCMPR HRHPSILRAC
     RLTVSAIECL TEETKSLNNG TTWQDLYTDE IREIISRSTV DSQLLKIEEI QEGDNDKMDF
     EQVFETLISI FKLHASEYSR VVILNFLNSP VFESKKVSKF FETLGRLQEL MYNLESVERL
     ALKTETKLSR NERKMDGKMK NKSLLELGWK QQTALALEAI LERLESESVT QSEVESALHK
     TFLVVKAEPA FPQPVKKIDV EVKNQDQKNP EVIVIEKGTG ERTDIDMVFE GTPLSEADKL
     SASKSAVARD VLLDGSEGRC HEASLFGELK MVLEPRRTDF AKRERTALAK FYGVDEHQLE
     QKEDEETFEA IASGDGEDPD PYDWRKDAEM SAGIHHDANN DDFLKSLKLR RVDDDIIE
 
 
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