Open ValWood opened 6 years ago
Mailed SGD as PMID:28727280 still isn't annotated
An excerpt:
This 2016 paper does not show it as a bona fida complex member. https://www.ncbi.nlm.nih.gov/pubmed/27381459 Other oddity is that the abstract reports a high similarity to a human protein, but this does not exist. This seems to be fungal specific (which is very rare for general TFs).
I will revert the PomBase annotation to "unknown" process
On 22/08/2018 09:47, Valerie Wood wrote:
Actually, I see what you mean. Although TFB6 is a component of the complex, it may not function in the context of transcription if it is ssl2 for use in other contexts.
only releasing On 22/08/2018 09:38, Valerie Wood wrote:
Hmm, not sure. I'm going to ask for advice on how others would annotate this. To me, it seems odd to say something is core TFIID, and then not have a transcription process based on this observation. But as you say the exact role in transcription is not established (I definitely wouldn't make a "NOT" annotation to show a lack of involvement based on the in vitro assay, because this does not rule out a role in transcription.....
On 17/08/2018 18:55, Rob Nash wrote:
Hi Val,
Thanks for clarifying and providing a possible paper to use in annotation. This subunit was identified much later than the rest of those for TFIID, and the gene/protein has not been well studied. I took a look at the paper you suggested, and in this paper they show no impact on in vitro transcriptional initiation or preinitiation complex (PIC) assembly. Add back experiments did not impact transcriptional initiation either. So I think this why we did not annotate the suggested process, and I am uncomfortable adding an IC followed by a NOT annotation.
The only observation of note in this paper is that in the presence of phosphorylated Tfb6p, the Ssl2p helicase subunit, tends to dissociate from TFIID and forms a heterodimer with Tfb6p. However, if Ssl2p is already assembled into a complete preinitation complex than Tfb6p appears unable to dissociate the helicase. So the only term I have been able come up would be this one:
GO:0034367 protein-containing complex remodeling The acquisition, loss, or modification of macromolecules within a complex, resulting in the alteration of an existing complex.
and the evidence is not strong. In the paper they basically study TFIID subunit composition in the absence and presence of TFB6, and then follow this up by add back experiments where some Ssl2p is now lost from TFIID and appears in complex with Tfb6p.
So I wonder if you have any thoughts on whether this would be an accurate annotation based on the evidence and of use to you. I am on the fence about adding this one.
Edith: "Yes, from that paper, I would agree that it is just suppression of a cold phenotype. I've removed that annotation and replaced it with GO:0010629 (Neg. regulation of gene expression, has_input PRP4|PRP3) since there's increase in PRP4 and PRP3 expression in a spp41 mutant."
So, this one will not be specific enough for our slim (could be txn, translation, processing, maturation). This one will come back into "unknowns"
rdl2,rbd4,rbd3,SPCC777.03 SPAC11D3.10 SPAC23A1.14 seem to be doing something together at the MOM (sulphur metabolism, folding? import? tRNA metabolism)
Done rdl2, could not track down the connection of annotation for the others
authors speculate oxidative phosphorylation, but really its more closely aligned with MAPK pathway and response to oxidative stress.
I've just done the community session for the ess1 paper
That's great. It's still unknown as I expected since its phenotypes not GO.
yup, and just H2O2 sensitivity at that.
done everything except SPBC21C3.17c waiting for response from SGD
SPBC21C3.17 can be annotated,
SGD annotated YKL077W to 'protein maturation'
Add back to unknowns. Transcription evidence very poor
obr1 / SPAC3C7.14c details back in unknown Poorly characterized
still to sort, conserved unknowns absent from OB list
SPBC25D12.06 | mitochondrial ATP-dependent RNA helicase (predicted) | |
---|---|---|
SPAC3A12.02 | mitochondrial inorganic diphosphatase (predicted) | |
SPAC12B10.14c | tea5 | pseudokinase Tea5 |
SPAC23A1.14c | pyridoxal phosphate-dependent transferase, unknown specificity, implicated in sulfur compound metabolis |
still to sort in OB unknowns list but not in PomBase unknown (conserved or species specific)
SPBC20F10.10 | psl1 | cyclin pho85 family Psl1 (predicted) |
---|---|---|
SPBP4G3.02 | pho1 | extracellular acid phosphatase Pho1 |
SPAC57A10.04 | mug10 | meiotic Rho guanine nucleotide exchange factor (predicted) |
Added back
Back in unknown.
SPBC17D11.08 dca7 WD repeat protein, DDB1 and CUL4-associated factor Dca7 (predicted)
added back, poorly characterised SPAC1B3.08
@bahler SPAC18B11.08c will come out of the conserved unknown list this week. It is PAT complex subunit Asterix (it is https://www.pombase.org/gene/SPBC2G5.01 CCCDC47 binding partner) PMID:32814900 PMID:33082068
removing mug151 from the conserved unknown list Seems to be ortholog of S. cerevisiae YMR263W previously was conserved in human but no S. cerevisiae ortholog /controlled_curation="term=orthologous to S. cerevisiae YMR263W; date=20210908"
/GO="aspect=C; term=nucleus; GOid=GO:0005634; evidence=ISS; db_xref=GO_REF:0000024; with=UniProtKB:Q02614; date=20060301" /GO="aspect=F; term=Rpd3L complex; GOid=GO:0033698; evidence=ISS; db_xref=GO_REF:0000024; with=SGD:S000004876; date=20210908" /GO="aspect=P; term=negative regulation of gene expression, epigenetic; GOid=GO:0045814; evidence=IC; db_xref=GO_REF:0000051; from=GO:0033698; date=20210908"
/product="Rpd3L complex subunit (predicted)" /primary_name="mug151" /systematic_id="SPAC3H1.03"
@bahler
for the record. From https://github.com/pombase/curation/issues/3089 https://www.pombase.org/gene/SPAC3H5.09c /product="ER-PM contact site phospholipid-binding protein Hob2 (predicted)" /GO="aspect=P; term=endoplasmic reticulum-plasma membrane tethering; GOid=GO:0061817; evidence=TAS; db_xref=PMID:34415038; date=20210823" /GO="aspect=F; term=protein-membrane adaptor activity; GOid=GO:0043495; annotation_extension=part_of(GO:0061817); evidence=TAS; db_xref=PMID:34415038; date=20210823" /GO="aspect=F; term=phosphatidylinositol binding; GOid=GO:0035091; evidence=TAS; db_xref=db_xref=PMID:34415038; date=20210823" /primary_name="hob2"
@bahler I don't know if I can make any GO annotation from this but /product="conserved eukaryotic protein, human C16orf72 ortholog" /systematic_id="SPAC6B12.14c" human ortholog is now named HAPSTR1 https://pubmed.ncbi.nlm.nih.gov/35776542/ and has some functional relationship with HUWE1 (ortholog of SPAC19D5.04) DUF4588
@bahler SPBC19G7.04 now annotated to PomBase SPBC19G7.04 GO:0106300 GO_REF:0000024 ISO Q96QF7 based on https://pubmed.ncbi.nlm.nih.gov/30914427/
Add back to unknowns SPAC1952.08c SPAC26F1.14c (aif1)
this is amazing synchronicity - i was recently looking at lipocalins 1 and 2! thank you xx
Another unknown published (coq12) | Identification of novel coenzyme Q10 biosynthetic proteins Coq11 and Coq12 in Schizosaccharomyces pombe. Nishida I, Ohmori Y, Yanai R, Nishihara S, Matsuo Y, Kaino T, Hirata D, Kawamukai M. J Biol Chem. 2023 May 6:104797. doi: 10.1016/j.jbc.2023.104797. Online ahead of print. PMID: 37156397
CC @bahler
@Antonialock this might be a nice project pathway.....
thank you! x
cqd1 UbiB protein kinase-like family member; mitochondrial inner membrane protein that interacts with outer membrane proteins Por1p and Om14p to form a MICOS-independent mitochondrial contact site; role in mitochondrial organization; contributes to mitochondrial lipid homeostasis; controls the cellular distribution of coenzyme Q (CoQ); contains a potential mitochondrial targeting sequence and predicted transmembrane domain
conserved "unknown" https://www.pombase.org/gene/SPBC21C3.03 https://www.biorxiv.org/content/10.1101/2022.04.09.487722v2.full.pdf+html
add name
Khosravi S, Chelius X, Unger AK, Rieger D, Frickel J, Sachsenheimer T, Lüchtenborg C, Schieweck R, Brügger B, Westermann B, Klecker T, Neupert W, Harner ME. | Related Articles | |
---|---|---|
The UbiB family member Cqd1 forms a novel membrane contact site in mitochondria. | ||
J Cell Sci. 2023 Apr 19;. [Epub ahead of print] | ||
PMID: 37073556 |
Also, this is cqd2 https://www.pombase.org/gene/SPBC15C4.02
An unknown protein spbc14C8.13 ber1 has been renamed as srr1
It was annotated SRR1 family protein, implicated in microtubule stabilization (yeast), and heme biosynthesis (mouse)
is now published in Fission yeast Srr1 and Skb1 promote isochromosome formation at the centromere PMID: 37237082
I don't know if we will get a GO process from the publication, so it could still be classed as "poorly characterized". This is a nice illustration of GO annotations in other species made from phenotypes which we would not make the corresponding inferred annotations. I think the only evidence for the yeast annotation was benomyl resistance. On its own this isn't enough to infer a GO process. We can only make annotations from phenotypes if we are confident the phenotype is specific for the process, OR if there are multiple lines of evidence.
Maybe its protein maturation since "The pattern of synthetic lethal interactions obtained with the ber1Δ mutant suggests that Ber1 may function in N-terminal protein acetylation."PMID: 18064466 A synthetic lethal screen approach suggested that Ber1 is implicated in a number of cellular functions, and most prominently in kinetochore function. Synthetic lethal screen analyses revealed that Rpn4, Ard1, Nat1 and Ber1 share a wide set of genetic interactions (Fig. 2). Our data therefore suggest that Ber1 may function in protein N-terminus acetylation and/or proteasome biogenesis. Since proteasome subunits are heavily N-acetylated (Csank et al. 2002), the role of Ber1 in proteasome assembly might be a secondary consequence of its role in protein modification. Thus, we suggest that Ber1 might be an accessory factor for the N-terminal acetyltransferase. We would however like to point out that with the currently available data this is only a working hypothesis.
3 more removed from the "conserved unknowns" list SPAC1687.14c Is now annotated to SPB organization by ISS SPAC23A1.14c Is now annotated to involved in sulfur compound metabolic process by ISS Atg44 is now annotated to mitophagy
I classed these as "known" according to our criteria, because they get annotated with GO processes via PAINT
SPBC106.03 mitochondrial Rossman fold DUF1776 family protein steroid metabolic process
https://www.pombase.org/gene/SPAC3H1.04c mitochondrial membrane organization
https://www.pombase.org/gene/SPBC216.03 Heme catabolism
https://www.pombase.org/gene/SPBC215.06c rRNA processing
Protein catabolic process https://www.pombase.org/gene/SPAC57A7.09 https://www.pombase.org/gene/SPAC3A12.03c
SPBC32H8.05 was conserved fungal unknown, now eukaryotically conserved
SPBC32H8.05 ribosome-associated protein, nucleolar, annotated to ribosome biogenesis
CONSERVED UNKNOWN CHANGES 410
Although these were in "conserved unknown" they had an existing process annotation and so they were not in the Open Biology unknown list:
removed from the open biology unknowns list since publcation, new gene characterizations
CURRENT TOTAL 406 (becasue some added back)
removed from the open biology unknowns list since publication, should not have been included
Added into conserved unknowns since publication, existing annotation removed
Added to conserved unknowns list (back from published or inferred) CRITERIA STRICTER, or they have a process annotation which resulted in them slimming despite being 'unknown'
SPECIES SPECIFIC UNKNOWNS CHARACTERIZED
ADDED TO SPECIES SPECIFIC UNKNOWNS gene | ID | comments | -- | -- sro1 | SPBC1347.11 | published, but no information about role prl46 |- new species specific protein
Misc oddity SPBPJ4664.02 (crazy cell surface protein) has adhesion but is still unknown really