Closed ValWood closed 4 years ago
add synonym exact decreased centromeric cohesion protection to FYPO:0006423
Actually this definition /term is a bit strange
abnormal chromosome segregation during meiosis I with split kinetochore and normal chromosome separation A cellular process phenotype in which kinetochores become separated during the first meiotic nuclear division, and in which homologous chromosomes are separated normally.
The homologous chromosome segregate normally
So that would be split kinetochore in meiosis I with equational homologous chromosome segregation
The phenotype is described by Yoshi as:
Abnormal chromosome segregation during meiosis II because of centromeric protection defects during meiosis I
Does that help
FYPO:0005633 indicates FYPO:0006423 ... How can we connect (or even merge) them?
If -- but only if -- the decreased cohesion represented by FYPO:0006423 is the only problem that can give rise to the segregation phenotype of FYPO:0005633, then we can add an "output" link (FYPO:0005633 output_of FYPO:0006423).
But before I do, please have a look at this comment from #2735 -- at that time, it looked like there might be more than one way to get sister chromatid separation in meiosis I. Is that still a concern?
The homologous chromosome segregate normally
No, they separate normally. Remember that GO BP defines segregation as the entire process, including chromosome condensation, cohesion, metaphase plate congression, etc. as well as separation. We discussed this at length in #2782 and #2783 (especially this comment, this one, and this one).
So that would be split kinetochore in meiosis I with equational homologous chromosome segregation
No, as above; in addition, equational segregation is not normal in meiosis I (it's normal in mitosis and meiosis II). Reductional segregation is normal for meiosis I. Also see FYPO:0005634, including the comment.
The phenotype is described by Yoshi as:
Abnormal chromosome segregation during meiosis II because of centromeric protection defects during meiosis I
Does that help
Sorry, no; if anything, it's more confusing now because everything prior to this comment mentions only meiosis I, and now this one brings up meiosis II as well.
note to self: change FYPO:0005633 name to avoid "split kinetochore" confusion; the comment even implies that's already been done!
centromeres are protected by cohesion in meiosis I so that they segregate normally in meiosis II.
Here the protection in meiosis I is abnormal (kinetochores separate in meiosis I). segregation at I (migration to the poles) was normal
however the lack of protection in meiosis I results in unequal segregation of sister chromatids in meiosis II -
Here the protection in meiosis I is abnormal (kinetochores separate in meiosis I).
Then not all of segregation was normal.
segregation at I (migration to the poles) was normal
Separation in meiosis I was normal.
however the lack of protection in meiosis I
To clarify: "protection" is a (slightly woollier) way of saying "sister chromatid cohesion"?
results in unequal segregation of sister chromatids in meiosis II -
OK, that's clearer in and of itself now. But I'm still a little hazy as to what it has to do with the initial summary for this ticket, since the two terms there only say anything about meiosis I.
Let's forget about the connection part for now.
I thought that separation referred to the release from the connection between chromosomes/chromatids (i.e cleavage cohesion) , and segregation was subsequent movement toward the poles?
I guess "protection" is the :maintenance of centromeric sister chromatid cohesion"? (the centromeric cohesion is actively maintained although the arms are cleaved)
correction I thought that separation referred to the release from the connection between chromosomes/chromatids (i.e cleavage cohesion) , and segregation was separation plus subsequent movement toward the poles?
and segregation was separation plus subsequent movement toward the poles?
see above ... or just look at GO
separation:
chromosome separation Biological Process
Definition (GO:0051304 GONUTS page) The cell cycle process in which paired chromosomes are detached from each other. Chromosome separation begins with the release of cohesin complexes from chromosomes; in budding yeast, this includes the cleavage of cohesin complexes along the chromosome arms, followed by the separation of the centromeric regions. Chromosome separation also includes formation of chromatid axes mediated by condensins, and ends with the disentangling of inter-sister catenation catalyzed by topoisomerase II (topo II). PMID:20352243
separation in meiosis I is abnormal because cohesin is cleaved at the centromeres and it shouldn't be.
Segregation is also abnormal I guess because separation is part_of segregation. But separation is more accurate.
Segregation at meiosis II is abnormal (unequal)
Segregation is also abnormal I guess because separation is part_of segregation.
Correct. That's why I can't put "normal segregation" in the names of terms like FYPO:0005633. But if "normal separation" includes the correct timing of cohesin cleavage, I should change "normal separation" to something else. "Reductional chromosome apportionment" would be accurate but unwieldy. I could use "normal outcome of chromosome separation", unless you think of something better.
Can't we say FYPO:0005633 "split kinetochore during meiosis I leading to unequal chromosome segregation at meiosis II?
I don't like it much.
In FYPO, terms with "split kinetochore" in the names now represent cases where a single kinetochore gets broken into parts (tho I only got round to mopping up FYPO:0005633 yesterday). For " premature sister kinetochore separation" terms, "split kinetochore" goes in related synonyms.
I'm really leery of building "leading to" into term definitions. It seems like there's a high risk of doing it wrongly, so as to create dodgy inferences. I could run the idea by @matentzn when he's back ... phenotype A leads to phenotype B is a challenge even when A and B are separate ontology classes.
oh, and 3. FYPO:0005633 has never had the faintest hint of meiosis II about it until now, so even if the "leading to" problem can be solved, is it really safe to rejig the existing term?
tangential note to self: open ticket to change terms added for #3290 - they're premature separation
In FYPO, terms with "split kinetochore" in the names now represent cases where a single kinetochore gets broken into parts (tho I only got round to mopping up FYPO:0005633 yesterday). For " premature sister kinetochore separation" terms, "split kinetochore" goes in related synonyms.
Great, I was just about to suggest we change this. I had already checked that all the annotations referred to the phenotype I tried to describe here. The authors call it split kinetochore so could this be a related synonym.
so
is it really safe to rejig the existing term?
yes. The other annotations are a single paper from Yoshi.
Could we do:
"premature kinetochore separation during meiosis with unequal chromosome segregation at meiosis II?
(so its two observations which occur in the same cell. We can lose the dependency)
OK, I used
premature sister kinetochore separation and normal chromosome division in meiosis I, and unequal sister chromatid segregation in meiosis II
and put your text in as an exact synonym
edit file: 48bb20dca3bc5c96c788dee0894d8586ea0770c6 release: 3d6d8217e41d38e07e812c7f918f3ea4487460dd
This phenotype
| 5 | abnormal chromosome segregation during meiosis I with split kinetochore and normal chromosome separation (FYPO:0005633) [single allele genotypes]
indicates
3 | decreased meiotic sister chromatid cohesion at centromere during meiosis I (FYPO:0006423) [single allele genotypes] | ...
basically " In moa1Δ cells, although a small population of cells underwent equa- tional segregation at meiosis I (because of defects in mono-orientation), the majority underwent reduc- tional segregation due to the presence of chiasmata and tension exerted across homologues (Fig. 1B). Strik- ingly, 22% of these ‘reductional’ moa1Δ cells showed the separation of imr1-GFP in prometaphase II (Fig. 1C). This separation value is significantly higher than in wild-type cells (<5%), although lower than in sgo1Δ cells (50%), in which cohesion protection is completely abolished (Fig. 1C). "
i.e the chromosomes do normal equational division because of chiasmata, but then "fall apart" because of a lack of centromeric cohesion
How can we connect (or even merge) them?